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Phenylphosphine information


Phenylphosphine
Names
Preferred IUPAC name
Phenylphosphane
Other names
Phenylphosphine
Monophenylphosphine
Identifiers
CAS Number
  • 638-21-1 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 12002 checkY
ECHA InfoCard 100.010.297 Edit this at Wikidata
EC Number
  • 211-325-4
PubChem CID
  • 12519
RTECS number
  • SZ2100000
UNII
  • 856X9KP929 checkY
UN number 2924
CompTox Dashboard (EPA)
  • DTXSID7073224 Edit this at Wikidata
InChI
  • InChI=1S/C6H7P/c7-6-4-2-1-3-5-6/h1-5H,7H2 ☒N
    Key: RPGWZZNNEUHDAQ-UHFFFAOYSA-N ☒N
  • InChI=1/C6H7P/c7-6-4-2-1-3-5-6/h1-5H,7H2
    Key: RPGWZZNNEUHDAQ-UHFFFAOYAH
SMILES
  • C1=CC=C(C=C1)P
Properties
Chemical formula
C6H5PH2
Molar mass 110.09 g/mol
Appearance Colorless liquid
Odor foul
Density 1.001 g/cm3
Boiling point 160 °C (320 °F; 433 K)
Hazards
GHS labelling:
Pictograms
GHS02: FlammableGHS06: ToxicGHS07: Exclamation mark
Signal word
Warning
Hazard statements
H250, H301, H311, H315, H319, H331, H335
Precautionary statements
P210, P222, P261, P264, P270, P271, P280, P301+P310, P302+P334, P302+P352, P304+P340, P305+P351+P338, P311, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P370+P378, P403+P233, P405, P422, P501
NIOSH (US health exposure limits):
PEL (Permissible)
none[1]
REL (Recommended)
C 0.05 ppm (0.25 mg/m3)[1]
IDLH (Immediate danger)
N.D.[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Phenylphosphine is an organophosphorus compound with the chemical formula C6H5PH2. It is the phosphorus analog of aniline. Like other primary phosphines, phenylphosphine has an intense penetrating odor and is highly oxidizable. It is mainly used as a precursor to other organophosphorus compounds. It can function as a ligand in coordination chemistry.

  1. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0501". National Institute for Occupational Safety and Health (NIOSH).

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Phenylphosphine

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Phenylphosphine is an organophosphorus compound with the chemical formula C6H5PH2. It is the phosphorus analog of aniline. Like other primary phosphines...

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Dichlorophenylphosphine

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Dichlorophenylphosphine is an organophosphorus compound with the formula C6H5PCl2. This colourless viscous liquid is commonly used in the synthesis of...

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PF

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located at KEK in Tsukuba, Japan pf(A), the Pfaffian of a matrix A Phenylphosphine, an organophosphorus compound Plasmodium falciparum, a species of Plasmodium...

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Tridentate ligand

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[(CH3)2NCH2CH2]2NCH3 3030-47-5 linear NNN 0 or +1 Li AlH2 Bis(diphenylphosphinoethyl)phenylphosphine Triphos 23582-02-7 linear PPP 0 transition metals 1,4,7-Trithiacyclononane...

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Parent structure

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inorganic chemistry. Phosphines Phosphine is the parent of phosphines. Phenylphosphine is a derivative of the parent phosphine. 3,3′,3′′-Phosphanetriyltris(benzenesulfonic...

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California Proposition 65 list of chemicals

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its salts – o-Phenylphenate, sodium 132-27-4 o-Phenylphenol 90-43-7 Phenylphosphine 638-21-1 PhiP (2-Amino-1-methyl-6-phenylimidazol[4,5-b]pyridine) 105650-23-5...

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Triphos

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1,1-Tris(diphenylphosphinomethyl)ethane Bis(diphenylphosphinoethyl)phenylphosphine This disambiguation page lists articles associated with the title Triphos...

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Organophosphine

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of dichlorophenylphosphine with lithium aluminium hydride affords phenylphosphine (PhPH2). Primary (RPH2) and secondary phosphines (RRPH and R2PH) add...

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Phosphinidene

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Hydrophosphination

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example is the Ti-catalyzed hydrophosphination of diphenylacetylene with phenylphosphine. This system involves a cationic catalyst precursor that is stabilized...

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List of compounds with carbon number 6

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isoniazid 54-85-3 C6H7N3O nicotinic acid hydrazide 553-53-7 C6H7P phenylphosphine 638-21-1 C6H7Si phenyl silyl radical 72975-30-5 C6H8 cyclopropylidene...

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