ChemicalBook--->CAS DataBase List--->1779-58-4

1779-58-4

1779-58-4 Structure

1779-58-4 Structure
IdentificationMore
[Name]

(Carbomethoxymethyl)triphenylphosphonium bromide
[CAS]

1779-58-4
[Synonyms]

CARBOMETHOXYMETHYL TRIPHENYLPHOSPHONIUM BROMIDE
(METHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
(2-methoxy-2-oxoethyl)triphenylphosphonium bromide
carbmethoxy Methyl Triphenyl Phosphonium Bromide
Carbomethoxymethyl triphenylphosphonium bromide, 98+%
methyl (triphenylphosphonio)acetate bromide
(METHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%
CMMTPPB
PHOSPHONIUM,(2-METHOXY-2-OXOETHYL)TRIPHENYL-,BROMIDE
(2-Oxo-2-methoxyethyl)triphenylphosphonium·bromide
Triphenyl(2-oxo-2-methoxyethyl)phosphonium·bromide
Triphenyl(methoxycarbonylmethyl)phosphonium·bromide
[EINECS(EC#)]

217-222-0
[Molecular Formula]

C21H20BrO2P
[MDL Number]

MFCD00011801
[Molecular Weight]

415.26
[MOL File]

1779-58-4.mol
Chemical PropertiesBack Directory
[Appearance]

white powder
[Melting point ]

165-170 °C (dec.) (lit.)
[storage temp. ]

2-8°C
[solubility ]

Soluble in methanol(almost transparency).
[form ]

solid
[Sensitive ]

Hygroscopic
[BRN ]

3812975
[InChIKey]

VCWBQLMDSMSVRL-UHFFFAOYSA-M
[CAS DataBase Reference]

1779-58-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[F ]

9
[HS Code ]

29319019
Hazard InformationBack Directory
[Chemical Properties]

white powder
[Uses]

(Methoxycarbonylmethyl)triphenylphosphonium bromide is a reactant for the synthesis of GSK-3 inhibitors using the Wittig reaction, substituted furanones for antifungal and cytostatic activities, photochromic dithienylethene derivatives, gem-diiodoalkanes containing allylic alcohols and highly substituted cyclopentenes and brazilanes via Au-catalyzed deoxygenative Nazarov cyclization. As reactant for asymmetric hydrogenation of α,β-unsaturated ester-phosphonates, studies of thermal decomposition of phosphonium alkyl ester salts.
[Purification Methods]

Wash it with pet ether (b 40-50o), recrystallise it from CHCl3/Et2O and dry it at high vacuum at 65o. [Isler et al. Helv Chim Acta 40 1242 1957, Wittig & Haag Chem Ber 88 1654, 1664 1955, Beilstein 16 IV 981.]
Spectrum DetailBack Directory
[Spectrum Detail]

(Carbomethoxymethyl)triphenylphosphonium bromide(1779-58-4)MS
(Carbomethoxymethyl)triphenylphosphonium bromide(1779-58-4)1HNMR
(Carbomethoxymethyl)triphenylphosphonium bromide(1779-58-4)IR1
(Carbomethoxymethyl)triphenylphosphonium bromide(1779-58-4)IR2
(Carbomethoxymethyl)triphenylphosphonium bromide(1779-58-4)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

(Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%(1779-58-4)
[Sigma Aldrich]

1779-58-4(sigmaaldrich)
[TCI AMERICA]

Methoxycarbonylmethyl(triphenyl)phosphonium Bromide,>97.0%(T)(1779-58-4)
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