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Acetone imine information


Acetone imine
Full structural formula of acetone imine with dimensions
Full structural formula of acetone imine with dimensions
Skeletal formula of acetone imine
Skeletal formula of acetone imine
Ball-and-stick model of acetone imine
Ball-and-stick model of acetone imine
Space-filling model of acetone imine
Space-filling model of acetone imine
Names
Preferred IUPAC name
Propan-2-imine[1]
Other names
  • Acetone imine
  • 2-Propanimine
Identifiers
CAS Number
  • 38697-07-3 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 125534 checkY
MeSH Imine Acetone Imine
PubChem CID
  • 142304
CompTox Dashboard (EPA)
  • DTXSID50191992 Edit this at Wikidata
InChI
  • InChI=1S/C3H7N/c1-3(2)4/h4H,1-2H3
    Key: XDAGXZXKTKRFMT-UHFFFAOYSA-N
SMILES
  • CC(=N)C
Properties
Chemical formula
C3H7N
Molar mass 57.096 g·mol−1
Appearance colorless liquid
Density 0.8 g cm−3 (25 °C)
Boiling point 57–59 °C (135–138 °F; 330–332 K)
log P -0.56
Refractive index (nD)
1.394
Hazards
GHS labelling:
Pictograms
GHS02: Flammable GHS07: Exclamation mark
Signal word
Danger
Hazard statements
H225, H319, H336
Precautionary statements
P210, P261, P305+P351+P338
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid
0
3
0
W
Flash point 14.7 °C (58.5 °F; 287.8 K)
Related compounds
Related compounds
Acetone oxime
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH3)2CNH. It is a volatile and flammable liquid at room temperature. It is the simplest ketimine. This compound is mainly of academic interest.

  1. ^ "Synonyms". Pubchem.

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Acetone imine

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Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH3)2CNH. It is a volatile and flammable liquid at room...

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Acetone azine

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also be produced from acetone (2 eq.), ammonia (2 eq.) and hydrogen peroxide (1 eq.). The first step is the formation of acetone imine, Me2C=NH; this is then...

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C3H7N

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The molecular formula C3H7N may refer to: Acetone imine Allylamine (2-propen-1-amine) Azetidine (trimethylenimine) Cyclopropylamine [de] 2-Methylaziridine...

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Ketone

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(which contains a carbon–oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH3)2CO. Many ketones are...

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Hexafluoroacetone

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chemical compound with the formula (CF3)2CO. It is structurally similar to acetone; however, its reactivity is markedly different. It a colourless, hygroscopic...

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Semicarbazone

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a derivative of imines formed by a condensation reaction between a ketone or aldehyde and semicarbazide. They are classified as imine derivatives because...

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Oxime

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In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and...

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Double bond

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oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O). In a skeletal formula, a double bond is drawn...

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Polyethylenimine

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or chloroform. It is insoluble in cold water, benzene, ethyl ether, and acetone. Linear polyethyleneimine has a melting point of around 67 °C. Both linear...

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Acetone oxime

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Acetone oxime (acetoxime) is the organic compound with the formula (CH3)2CNOH. It is the simplest example of a ketoxime. It is a white crystalline solid...

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Peroxide process

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individual steps are as follows. Imine formation through condensation: Me(Et)C=O + NH3 → Me(Et)C=NH + H2O Oxidation of the imine to the oxaziridine: Me(Et)C=NH...

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Tropinone

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Intermolecular Mannich reaction of the enolate of acetone dicarboxylate New enolate formation and new imine formation with loss of water for Second intramolecular...

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Ketene

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beta-lactones. With imines, beta-lactams are formed. This is the Staudinger synthesis, a facile route to this important class of compounds. With acetone, ketene reacts...

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Transfer hydrogenation

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ketones and imines to alcohols and amines, respectively. The hydrogen-donor (transfer agent) is typically isopropanol, which converts to acetone upon donation...

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Trifluoroacetone

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less prone to hydrate than hexafluoroacetone and more electrophilic than acetone itself. Unlike both of those ketones, trifluoroacetone is prochiral. Hydrogenation...

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Feprosidnine

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is a mesoionic sydnone imine. A similar agent is described in the Amfetaminil article. Base catalyzed reaction between acetone cyanohydrin and 40% formaldehyde...

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Hydrazone

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Selected parameters: C=N, 128 pm; N-N, 138 pm, N-N-C(Ar), 119 pm Azo compound Imine Nitrosamine Hydrogenation of carbon–nitrogen double bonds March, Jerry (1985)...

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Hydrogenation

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hydrogenation of phenylacetylene using the Lindlar catalyst. Hydrogenation of an imine using a Raney nickel catalyst, a popular heterogeneous catalyst. Partial...

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Methoxyamine

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hydroxylamine, methoxyamine condenses with ketones and aldehydes to give imines. Methoxyamine is used as a synthon for NH2+. It undergoes deprotonation...

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Beckmann rearrangement

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rearrangement occurs stereospecifically for ketoximes and N-chloro/N-fluoro imines, with the migrating group being anti-periplanar to the leaving group on...

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Ethanimine

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Ethanimine is an organonitrogen compound classified as an imine. It is formed by reacting acetaldehyde and ammonia, but rapidly polymerizes to acetaldehyde...

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Organic peroxides

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Methyl ethyl ketone peroxide, benzoyl peroxide and to a smaller degree acetone peroxide are used as initiators for radical polymerization of some thermosets...

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Isoquinoline

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platelets that have a low solubility in water but dissolve well in ethanol, acetone, diethyl ether, carbon disulfide, and other common organic solvents. It...

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Chichibabin pyridine synthesis

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paraldehyde and ammonia. These syntheses involve many reactions such as imine synthesis, base-catalyzed aldol condensations, and Michael reactions. Many...

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Acetal

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sometimes called a formal or the methylenedioxy group. The acetal formed from acetone is sometimes called an acetonide. Used in a more general sense, the term...

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Hydrazine

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carbonyl is its reaction with acetone to give the acetone azine. The latter reacts further with hydrazine to yield acetone hydrazone: 2 (CH3)2CO + N2H4...

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Carbonyl group

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within a carbonyl compound decreases. The pKa values of acetaldehyde and acetone are 16.7 and 19 respectively, Infrared spectroscopy: the C=O double bond...

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