140195-93-3

Basic information

• Product Name: Cyclopropanecarboxylic acid, 1-[[[[(phenylmethoxy)carbonyl]amino]acetyl]amino]-, ethyl ester
• CAS NO: 140195-93-3
• Molecular Formula: C16H20N2O5
• Molecular Weight: 320.345
• Mol File: 140195-93-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclopropanecarboxylic acid, 1-[[[[(phenylmethoxy)carbonyl]amino]acetyl]amino]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-[[[[(phenylmethoxy)carbonyl]amino]acetyl]amino]-, ethyl ester(140195-93-3)
• EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-[[[[(phenylmethoxy)carbonyl]amino]acetyl]amino]-, ethyl ester(140195-93-3)

Safety Data

• Hazardous Substances Data: 140195-93-3(Hazardous Substances Data)

Upstream product

• 2899-60-7 Cbz-Gly-ONSuc 
• 72784-47-5 ethyl 1-aminocyclopropane-1-carboxylate 
• 82997-99-7 Ethyl 1-azidocyclopropanecarboxylate 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 42303-42-4 ethyl 1-aminocyclopropanecarboxylate hydrochloride 

Downstream Products

• 145256-97-9 1-(2,4-difluorophenyl)-6-fluoro-7-(4,7-diazaspiro<2,5>octan-7-yl)-1,4-dihydro-4-oxo<1,8>naphthyridine-3-carboxylic acid trifluoroacetic acid salt 
• 145122-69-6 ethyl 1-(2,4-difluorophenyl)-6-fluoro-7-(4,7-diazaspiro<2,5>octan-7-yl)-1,4-dihydro-4-oxo<1,8>naphthyridine-3-carboxylate 
• 145122-56-1 4,7-diazaspiro<2,5>octane dihydrochloride 
• 129306-17-8 4,7-diazaspiro[2.5]octane-5,8-dione 
• 145122-57-2 3-Oxo-[1,4]diazepane-5-carboxylic acid ethyl ester 

Relevant articles and documents

UREA DERIVATIVES AS PYRUVATE KINASE ACTIVATORS

The subject matter described herein is directed to pyruvate kinase activating compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for the treatment of diseases associated with PKR and/or PKM2, such as pyruvate kinase deficiency, sickle cell disease, and beta-thalassemia.

A fast procedure for the preparation of amides/peptides from carboxylic acids and azides via two redox reactions: Application to the synthesis of methionine enkephalin

A one-pot self regulated approach for the synthesis of amides/peptides based on two reduction-oxidation (redox) reactions has been described. The primary and secondary amides/peptides are made by using azidotrimethylsilane and alkyl azides/α-azido acid de

Syntheses and antibacterial activity of novel 6-fluoro-7-(gem-disubstituted piperazin-1-yl)-quinolines

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