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
  • benzyl N-(3-butanoylphenyl)carbamate
  • Benzyl 8-hydroxy-3-methyl-1,2,3,4-tetrahydroquinoline-1-carboxylate
  • (S)-(1-benzofuran-2-yl)(cyclopentyl)methanamine
  • benzyl N-{6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-8-yl}carbamate
  • benzyl N-(5-acetyl-2-chlorophenyl)carbamate
  • benzyl N-[2-(3,5-dimethyl-1H-pyrazol-1-yl)-6-methylpyrimidin-4-yl]-N-(2-hydroxyethyl)carbamate
  • benzyl N-[3-(4-chlorophenoxy)-5-nitrophenyl]carbamate
  • Methyl 4-bromo-2-{[(tert-butoxy)carbonyl]amino}-3,5-dichlorobenzoate
  • benzyl N-[6-(3-bromophenoxy)pyridin-3-yl]carbamate
  • 2-{5-bromo-1-[(prop-2-en-1-yloxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid