di-t-butylmethylphosphine

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Names

[ CAS No. ]:
6002-40-0

[ Name ]:
di-t-butylmethylphosphine

[Synonym ]:
ditert-butyl(methyl)phosphane
MFCD01634711

Chemical & Physical Properties

[ Density]:
0.824 g/mL at 25ºC(lit.)

[ Boiling Point ]:
58ºC12 mm Hg(lit.)

[ Molecular Formula ]:
C9H21P

[ Molecular Weight ]:
160.23700

[ Flash Point ]:
60ºC

[ Exact Mass ]:
160.13800

[ PSA ]:
13.59000

[ LogP ]:
3.69510

[ Appearance of Characters ]:
liquid | colorless

[ Storage condition ]:
Flammables area

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H250-H314

[ Precautionary Statements ]:
P222-P231-P280-P305 + P351 + P338-P310-P422

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

[ Hazard Codes ]:
F,C

[ Risk Phrases ]:
17-34

[ Safety Phrases ]:
S16-S26-S45-S36-S37-S39

[ RIDADR ]:
UN 2845 4.2/PG 1

[ WGK Germany ]:
3

[ HS Code ]:
2901100000

Synthetic Route

Customs

[ HS Code ]: 2901100000

[ Summary ]:
2901100000 saturated acyclic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0%

Articles

Room-temperature Hiyama cross-couplings of arylsilanes with alkyl bromides and iodides.

J. Am. Chem. Soc. 125 , 5616, (2003)

The first method for achieving Hiyama couplings of unactivated alkyl bromides and iodides is reported. The desired carbon-carbon bond formation proceeds under mild conditions (room temperature) with g...


More Articles


Related Compounds

  • di-t-butyl benzylmalonate
  • Di-t-butylphosphinoferrocene tetrafluoroborate
  • Di-t-butylacetylene
  • Di-t-butyl(n-butyl)phosphine, Min. 97
  • Di-t-butylzinndihydroxid
  • di-t-Bu-XPhos
  • Methyl 6-isopropyl-3-(pyrimidin-5-ylamino)pyrazine-2-carboxylate
  • 1-(2-Methoxyethyl)-N-methyl-4-nitro-1H-pyrazole-5-carboxamide
  • N-((4-phenyl-1H-imidazol-2-yl)methyl)quinoxalin-2-amine
  • 2,2,5,5-Tetramethyloxolane-3-carbonitrile
  • 4-Acetyl-6-fluoropyridine-2-carboxylic acid
  • 7,8-dimethoxy-2-(2-oxo-2-{4-[2-(4-pyridyl)ethyl]piperazino}ethyl)-1(2H)-phthalazinone
  • N8-(Cyclopropylmethyl)-N4-[3-(methylthio)phenyl]-2-(1-piperazinyl)pyrimido[5,4-d]pyrimidine-4,8-diamine
  • 2-(3,4-Dimethoxyphenethyl)-7-(4-fluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine
  • 2-bromo-5-isopropyl-N-[2-(1,3-thiazol-2-yl)ethyl]-1,3-thiazole-4-carboxamide
  • 2-(7,8-dimethoxy-2-oxo-1,2-dihydro-3H-3-benzazepin-3-yl)-N-(2-ethoxyphenyl)acetamide
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