92789-04-3

Basic information

• Product Name: Hydrazinecarboxylic acid, 2-benzoyl-, 1,1-dimethylethyl ester
• CAS NO: 92789-04-3
• Molecular Formula: C12H16N2O3
• Molecular Weight: 236.271
• Mol File: 92789-04-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Hydrazinecarboxylic acid, 2-benzoyl-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-benzoyl-, 1,1-dimethylethyl ester(92789-04-3)
• EPA Substance Registry System: Hydrazinecarboxylic acid, 2-benzoyl-, 1,1-dimethylethyl ester(92789-04-3)

Safety Data

• Hazardous Substances Data: 92789-04-3(Hazardous Substances Data)

Upstream product

• 870-46-2 t-butoxycarbonylhydrazine 
• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 
• 108732-34-9 benzoic acid isobutoxycarbonyl ester 
• 93-89-0 benzoic acid ethyl ester 

Downstream Products

• 1452-58-0 benzoic hydrazide hydrochloride 
• 50996-03-7 benzamidoacetone 
• 170384-29-9 (+/-)-1-(N-tert-Butoxycarbonylamino)propan-2-one 
• 304667-32-1 N'-(2-nitrobenzenesulfonyl)benzhydrazide 
• 1157-84-2 (E)-1-benzylidene-2-(2,4-dinitrophenyl)hydrazine 
• 7031-95-0 1-benzoxy-2,2,6,6-tetramethylpiperidine 
• 613-94-5 benzoic acid hydrazide 
• 92959-54-1 N₁-benzoyl-N₂-tert-butoxycarbonyldiazene 

Relevant articles and documents

Carboxyesterase polypeptides for amide coupling

The present invention provides engineered carboxyesterase enzymes having improved properties as compared to a naturally occurring wild-type carboxyesterase enzymes, as well as polynucleotides encoding the engineered carboxyesterase enzymes, host cells capable of expressing the engineered carboxyesterase enzymes, and methods of using the engineered carboxyesterase enzymes in amidation reactions.

An open-source approach to automation in organic synthesis: The flow chemical formation of benzamides using an inline liquid-liquid extraction system and a homemade 3-axis autosampling/product-collection device

Several open-source hardware and software technologies (RAMPS, Python, PySerial, OpenCV) were used to control an automated flow chemical synthesis system. The system was used to effect the synthesis of a series of benzamides. An inexpensive Raspberry Pi single board computer provided an electronic interface between the control computer and the RAMPS motor driver boards.

Triazole derivatives as non-nucleoside inhibitors of HIV-1 reverse transcriptase-Structure-activity relationships and crystallographic analysis

A series of 3,4,5-trisubstituted 1,2,4-4H triazole derivatives was synthesized and investigated for HIV-1 reverse transcriptase inhibition. An X-ray structure with HIV-1 RT secured the binding mode and allowed the key interactions with the enzyme to be identified.