Home > Compound List > Product Information
(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide_Molecular_structure_CAS_52509-14-5)
Click picture or here to close

(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide

Catalog No. 223859 Name Sigma Aldrich
CAS Number 52509-14-5 Website http://www.sigmaaldrich.com
M. F. C22H22BrO2P Telephone 1-800-521-8956
M. W. 429.286641 Fax
Purity 98% Email
Storage Chembase ID: 82207

SYNONYMS

Title
(1,3-二氧环戊基-2-甲基)三苯基溴化膦
IUPAC name
(1,3-dioxolan-2-ylmethyl)triphenylphosphanium bromide
IUPAC Traditional name
(1,3-dioxolan-2-ylmethyl)triphenylphosphanium bromide

DATABASE IDS

EC Number 257-977-3
MDL Number MFCD00011966
PubChem SID 24853408
CAS Number 52509-14-5

PROPERTIES

Safety Statements 26-37/39
German water hazard class 3
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H312-H315-H319-H332-H335
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P280-P305 + P351 + P338
Risk Statements 20/21/22-36/37/38
Empirical Formula (Hill Notation) C22H24BrO2P
Purity 98%
Melting Point 193-195 °C(lit.)

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application
Reactant for:
• Preparation of a ratiometric fluorescent probe for specific detection of cysteine over homocysteine and glutathione1
• Microwave-assisted synthesis of KN-93 as inhibitor of calmodulin kinase II2
• Preparation of fluorinated spirobenzofuran piperidines as s1 receptor ligands3
• Synthesis and antitumor agents4
• Regio-selective preparation of indole derivatives via rhodium-catalyzed domino hydroformylation/indolization5
Description (简体中文)
包装
5 g in glass bottle
Application
Reactant for:
• Preparation of a ratiometric fluorescent probe for specific detection of cysteine over homocysteine and glutathione1
• Microwave-assisted synthesis of KN-93 as inhibitor of calmodulin kinase II2
• Preparation of fluorinated spirobenzofuran piperidines as s1 receptor ligands3
• Synthesis and antitumor agents4
• Regio-selective preparation of indole derivatives via rhodium-catalyzed domino hydroformylation/indolization5

REFERENCES