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(3-Carboxypropyl)triphenylphosphonium bromide_Molecular_structure_CAS_17857-14-6)
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(3-Carboxypropyl)triphenylphosphonium bromide

Catalog No. 349720 Name Sigma Aldrich
CAS Number 17857-14-6 Website http://www.sigmaaldrich.com
M. F. C22H22BrO2P Telephone 1-800-521-8956
M. W. 429.286641 Fax
Purity 98% Email
Storage Chembase ID: 74358

SYNONYMS

Title
(3-羧丙基)三苯基溴化膦
IUPAC name
(3-carboxypropyl)triphenylphosphanium bromide
IUPAC Traditional name
(3-carboxypropyl)triphenylphosphanium bromide
Synonyms
(4-Hydroxy-4-oxobutyl)triphenylphosphonium bromide

DATABASE IDS

CAS Number 17857-14-6
MDL Number MFCD00274196
PubChem SID 24861704

PROPERTIES

Linear Formula HO2C(CH2)3P(C6H5)3Br
Purity 98%
Melting Point 244-247 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
25, 100 g in glass bottle
Application
Reactant for preparation of:
• Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity1
• Boron-containing benzoxaboroles as antimalarial agents2
• Methyl alkenyl quinolones as antimycobacterial agents3
• Solandelactone E via Sharpless epoxidation, Taber cyclopropanation, chemoselective reductions and lithiation-borylation-allylation sequence4
• Organotin compounds as antifungal agents5
• Oleanolic acid derivatives as inhibitors of protein tyrosine phosphatase 1B for negative regulation of insulin pathway (a promising target for treatment of diabetes and obesity)6
• 11-oxa prostaglandin analogs with ocular hypotensive activity7
Description (简体中文)
包装
25, 100 g in glass bottle
Application
Reactant for preparation of:
• Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity1
• Boron-containing benzoxaboroles as antimalarial agents2
• Methyl alkenyl quinolones as antimycobacterial agents3
• Solandelactone E via Sharpless epoxidation, Taber cyclopropanation, chemoselective reductions and lithiation-borylation-allylation sequence4
• Organotin compounds as antifungal agents5
• Oleanolic acid derivatives as inhibitors of protein tyrosine phosphatase 1B for negative regulation of insulin pathway (a promising target for treatment of diabetes and obesity)6
• 11-oxa prostaglandin analogs with ocular hypotensive activity7

REFERENCES