497155-23-4

Basic information

• Product Name: Hydrazinecarboxylic acid, 2-[carboxy(4-methoxyphenyl)methyl]-2-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester
• CAS NO: 497155-23-4
• Molecular Formula: C21H26N2O5
• Molecular Weight: 386.448
• Mol File: 497155-23-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Hydrazinecarboxylic acid, 2-[carboxy(4-methoxyphenyl)methyl]-2-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-[carboxy(4-methoxyphenyl)methyl]-2-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester(497155-23-4)
• EPA Substance Registry System: Hydrazinecarboxylic acid, 2-[carboxy(4-methoxyphenyl)methyl]-2-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester(497155-23-4)

Safety Data

• Hazardous Substances Data: 497155-23-4(Hazardous Substances Data)

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 6000-59-5 glyoxalic acid monohydrate 
• 53370-84-6 N'-benzylhydrazinecarboxylic acid tert-butyl ester 
• 298-12-4 Glyoxilic acid 

Relevant articles and documents

One-pot synthesis of new fused 4,5-bridged l,2,5-triazepine-3,6-diones, l,2,5-triazepine-3,7-diones heterocycles by Petasis reaction

The one pot synthesis of a new fused l,2,5-triazepine-3,6-diones, l,2,5-triazepine-3,7-diones heterocyles has been described via Petasis reactions. These heterocycles might be suitable for elaboration into larger peptides at amino termini. The scope and limitations of this method have been examined.

Petasis boronic acid-Mannich reactions of substituted hydrazines: Synthesis of α-hydrazinocarboxylic acids

N-1-(Carbamate protected)-N-2-(alkyl or aryl substituted) hydrazines can serve as amine substrates for the Petasis boronic acid-Mannich reaction, providing a practical synthetic route for the preparation of α-hydrazinocarboxylic acids. The scope and limitations of this method have been examined.