dimethylphenylphosphine

Names

[ CAS No. ]:
672-66-2

[ Name ]:
dimethylphenylphosphine

[Synonym ]:
Dimethylphenylphosphine
EINECS 211-595-3
MFCD00008509
dimethyl(phenyl)phosphane

Chemical & Physical Properties

[ Density]:
0.971 g/mL at 25 °C(lit.)

[ Boiling Point ]:
74-75 °C12 mm Hg(lit.)

[ Melting Point ]:
126-127ºC

[ Molecular Formula ]:
C₈H₁₁P

[ Molecular Weight ]:
138.14700

[ Flash Point ]:
122 °F

[ Exact Mass ]:
138.06000

[ PSA ]:
13.59000

[ LogP ]:
2.05340

[ Vapour Pressure ]:
11 mm Hg ( 68 °C)

[ Index of Refraction ]:
n20/D 1.563(lit.)

[ Storage condition ]:
Flammables area

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R10

[ Safety Phrases ]:
S26-S36-S16

[ RIDADR ]:
UN 1993 3/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
6.1

[ HS Code ]:
2902909090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2902909090

[ Summary ]:
2902909090 other aromatic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0%

Articles

Facile construction of macroporous hybrid monoliths via thiol-methacrylate Michael addition click reaction for capillary liquid chromatography.

J. Chromatogr. A. , doi:10.1016/j.chroma.2014.12.031, (2014)

A facile approach based on thiol-methacrylate Michael addition click reaction was developed for construction of porous hybrid monolithic materials. Three hybrid monoliths were prepared via thiol-metha...

Dimethylphenylphosphine oxide
Dimethylphenylphosphine borane
[W(dimethylphenylphosphine)3H6]
[Mo(dimethylphenylphosphine)4H4]
(dimethylphenylphosphine)iodogold(I)
Ni(SC6H5)2(dimethylphenylphosphine)2
N-(2,6-difluorobenzyl)-2-[4-(2-methyl-2H-tetrazol-5-yl)phenoxy]acetamide
5-fluoro-N-{3-[1-(2-methylpropyl)-1H-benzimidazol-2-yl]propyl}-2-(1H-tetrazol-1-yl)benzamide
2-methyl-N-[3-(1-methyl-1H-benzimidazol-2-yl)propyl]-5-(propan-2-yl)-1,3-thiazole-4-carboxamide
N-[2-(1H-benzimidazol-2-yl)ethyl]-4-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)butanamide
3,4-dimethyl-N-(2,3,4,9-tetrahydro-1H-carbazol-1-yl)-2-(1H-tetrazol-1-yl)benzamide
methyl 4-(2-methoxy-2-oxoethyl)-2-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}-1,3-thiazole-5-carboxylate
4-(4-methoxyphenyl)-N-{[1-(propan-2-yl)-1H-benzimidazol-2-yl]methyl}tetrahydro-2H-pyran-4-carboxamide
N-[(1-methyl-1H-benzimidazol-2-yl)methyl]tetrazolo[1,5-a]pyridine-7-carboxamide
N-[2-(1H-indol-3-yl)ethyl]-4-[2-(propan-2-yl)-2H-tetrazol-5-yl]benzamide
N-[3-(1-methyl-1H-benzimidazol-2-yl)propyl]-1-(pyrimidin-2-yl)piperidine-3-carboxamide

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