methyltriphenoxyphosphonium iodide

Suppliers

Names

[ CAS No. ]:
17579-99-6

[ Name ]:
methyltriphenoxyphosphonium iodide

[Synonym ]:
MFCD00011911
methyl(triphenoxy)phosphanium,iodide
EINECS 241-551-9
Methyltriphenoxyphosphonium iodide

Chemical & Physical Properties

[ Melting Point ]:
142-146ºC(lit.)

[ Molecular Formula ]:
C19H18IO3P

[ Molecular Weight ]:
452.22300

[ Exact Mass ]:
452.00400

[ PSA ]:
41.28000

[ LogP ]:
2.61980

[ Appearance of Characters ]:
solid

[ Storage condition ]:
0-6°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2931900090

Synthetic Route

Precursor & DownStream

Precursor

  • Triphenyl phosphite
  • methyl iodide

DownStream

  • 4-(Iodomethyl)-2,2-dimethyl-1,3-dioxolane
  • diphenyl methylphosphonate
  • methyltetraphenoxyphosphorane
  • N,N-Dimethylformamide
  • methyl iodide
  • Ethyl iodide
  • Phenol
  • 7,7-diphenyl-4-thia-1,6-diazabicyclo[3.3.0]oct-5-ene

Customs

[ HS Code ]: 2931900090

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Articles

C.W. Spangler et al.

J. Chem. Soc. Perkin Trans. I , 2287, (1981)

B.R. Castro

Org. React. 29 , 1, (1983)

K. Yamada et al.

J. Org. Chem. 43 , 2076, (1978)


More Articles


Related Compounds

  • methyltriphenoxyphosphonium trifluoromethanesulfonate
  • tetraethylarsanium,iodide
  • hafnium iodide
  • pentylmagnesium iodide
  • dibenziodolium, iodide
  • Sodium iodide
  • 2-(2-{[1-benzyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pyrrolidin-3-yl]formamido}ethoxy)acetic acid
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methoxybutanoyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylhexanoyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[1-benzyl-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidine-4-carbonyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[5-cyano-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • 2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylpropanoyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid
  • (2R)-1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4,4-difluorobutanoyl]piperidine-2-carboxylic acid
  • 4-{[(2,5-dimethyl-1H-imidazol-4-yl)methyl]carbamoyl}-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid
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