19791-95-8

Basic information

• Product Name: α-hydroxyhippuric acid
• CAS NO: 19791-95-8
• Molecular Weight: 195.175
• Mol File: 19791-95-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: α-hydroxyhippuric acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-hydroxyhippuric acid(19791-95-8)
• EPA Substance Registry System: α-hydroxyhippuric acid(19791-95-8)

Safety Data

• Hazardous Substances Data: 19791-95-8(Hazardous Substances Data)

Upstream product

• 495-69-2 Hippuric Acid 
• 55-21-0 benzamide 
• 563-96-2 2,2-dihydroxyacetic acid 
• 56-23-5 tetrachloromethane 
• 7726-95-6 bromine 
• 1199-01-5 2-phenylazlactone 
• 107-06-2 1,2-dichloro-ethane 
• 298-12-4 Glyoxilic acid 
• 546-67-8 lead(IV) tetraacetate 
• 71-43-2 benzene 

Downstream Products

• 62804-58-4 methyl 2-benzoylamino-4-oxopentanoate 
• 58486-97-8 2-Benzamido-4-oxopentansaeure,N-Benzoyl-β-acetylalanin 
• 56674-30-7 2-(benzamido)-2-(4-methoxyphenyl) acetic acid 
• 67809-31-8 N-Benzoyl-β,β-dibenzoyl-alanin 
• 56538-65-9 benzoylamino-benzylsulfanyl-acetic acid 
• 153397-36-5 N-Benzoyl-α-(3,4-dimethoxyphenyl)glycine 
• 56713-47-4 N-Benzoyl-2-hydroxy-5-chlorphenylglycin 
• 1451092-79-7 N-(5-bromo-2-oxo-2,3-dihydrobenzofuran-3-yl)benzamide 
• 1451092-80-0 N-(5-chloro-2-oxo-2,3-dihydrobenzofuran-3-yl)benzamide 
• 1451092-81-1 N-(5-fluoro-2-oxo-2,3-dihydrobenzofuran-3-yl)benzamide 
• 872513-93-4 (2S)-methyl 2-N-benzoylamino-5-methylhex-4-enoate 
• 947154-84-9 (2S)-6-acetoxy-2-benzoylamino-4-hexenoic acid methyl ester 
• 947154-56-5 (2Z)-methyl 2-N-benzoylamino-5-methylhexa-2,4-dienoate 
• 947154-90-7 (2R)-methyl 2-N-benzoylamino-5-methylhex-4-enoate 

Relevant articles and documents

Methods for the synthesis of dicarba bridges in organic compounds

The present invention relates to methods for forming dicarba bridges in organic compounds. This involves the use of a pair of complementary metathesisable groups on the organic compound, and subjecting the compound to cross-metathesis under microwave radiation conditions. In an alternative, the compounds contain a turn-inducing group between the pair of cross-metathesisable groups to facilitate the cross-metathesis.

Conotoxin analogues and methods for synthesis of intramolecular dicarba bridge-containing peptides

According to the present invention, there is provided a range of new conotoxin derivatives and methods for synthesizing these analogues and other intramolecular dicarba bridge-containing peptides, including dicarba-disulfide bridge-containing peptides.