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2-(Diphenylphosphino)terephthalic acid 1-methyl 4-pentafluorophenyl diester_Molecular_structure_CAS_)
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2-(Diphenylphosphino)terephthalic acid 1-methyl 4-pentafluorophenyl diester

Catalog No. 679011 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C27H16F5O4P Telephone 1-800-521-8956
M. W. 530.379317 Fax
Purity 97% Email
Storage Chembase ID: 139804

SYNONYMS

Title
2-(二苯基膦)对苯二甲酸 1-甲基 4-五氟苯基二酯
IUPAC name
1-methyl 4-pentafluorophenyl 2-(diphenylphosphanyl)benzene-1,4-dicarboxylate
IUPAC Traditional name
1-methyl 4-pentafluorophenyl 2-(diphenylphosphanyl)benzene-1,4-dicarboxylate
Synonyms
1-Methyl-4-(pentafluorophenyl)-2-(diphenylphosphino)-1,4-benzenedicarboxylate
1-甲基-4-(五氟苯基)-2-(二苯基膦)-1,4-苯二羧酸酯

DATABASE IDS

PubChem SID 24885463
MDL Number MFCD09265125

PROPERTIES

Empirical Formula (Hill Notation) C27H16F5O4P
Purity 97%
Melting Point 109-111 °C
MSDS Link Download
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Packaging
25, 100 mg in glass bottle
Application

• Staudinger ligation reagent for the conjugation of amine and azide containing compounds or biomolecules.
• The amine functionalized molecule first reacts with the phosphine through the activated pentafluorophenyl ester.The azide-molecule is then reacted with the newly labeled phosphine to form the iminophosphorane, and the aza-ylide is subsequently captured by the methyl ester to yield the covalent conjugated product.1The Staudinger Ligation: A High-Yield, Chemoselective, and Mild Synthetic Method
Description (简体中文)
包装
25, 100 mg in glass bottle
Application

• Staudinger ligation reagent for the conjugation of amine and azide containing compounds or biomolecules.
• The amine functionalized molecule first reacts with the phosphine through the activated pentafluorophenyl ester.The azide-molecule is then reacted with the newly labeled phosphine to form the iminophosphorane, and the aza-ylide is subsequently captured by the methyl ester to yield the covalent conjugated product.1The Staudinger Ligation: A High-Yield, Chemoselective, and Mild Synthetic Method

REFERENCES