missing translation for 'onlineSavingsMsg'
Learn More

(Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%

CAS: 1779-58-4 | C21H20BrO2P | 415.27 g/mol

$66.75 - $587.00

Chemical Identifiers

CAS 1779-58-4
Molecular Formula C21H20BrO2P
Molecular Weight (g/mol) 415.27
MDL Number MFCD00011801
InChI Key VCWBQLMDSMSVRL-UHFFFAOYSA-M
Synonym 2-methoxy-2-oxoethyl triphenylphosphonium bromide, methoxycarbonylmethyl triphenylphosphonium bromide, carbomethoxymethyl triphenylphosphonium bromide, methoxycarbonylmethyl triphenyl phosphonium bromide, 2-methoxy-2-oxoethyl triphenylphosphanium bromide, 2-methoxy-2-oxoethyl-triphenylphosphanium bromide, 2-methoxy-2-oxo-ethyl-triphenyl-phosphonium bromide, phosphonium, 2-methoxy-2-oxoethyl triphenyl-, bromide, acmc-209edxShow MoreShow Less
PubChem CID 2733211
IUPAC Name (2-methoxy-2-oxoethyl)-triphenylphosphanium;bromide
SMILES [Br-].COC(=O)C[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
View More Specs

Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1630114
View Documents
Thermo Scientific Chemicals
A1630114
25 g
Each for $66.75
Only null left
 
AAA1630122
View Documents
Thermo Scientific Chemicals
A1630122
100 g
Each for $186.12
Only null left
 
AAA1630136
View Documents
Thermo Scientific Chemicals
A1630136
500 g
Each for $587.00
Only null left
 
Description

Description

(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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(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.

Solubility
Soluble in methanol(almost transparency).

Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
Specifications
Show More
Videos
Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 217-222-0

TSCA : No

Recommended Storage : Ambient temperatures

SDS
missing translation for 'documents'

missing translation for 'documents'

RUO – Research Use Only