6959-76-8

Basic information

• Product Name: N-[4-(ethoxycarbonyl)phenyl]-beta-alanine
• CAS NO: 6959-76-8
• Molecular Formula: C₁₂H₁₅NO₄
• Molecular Weight: 237.2518
• Mol File: 6959-76-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 443.4°C at 760 mmHg
• Flash Point: 221.9°C
• Density: 1.242g/cm³
• Vapor Pressure: 1.22E-08mmHg at 25°C
• Refractive Index: 1.575
• CAS DataBase Reference: N-[4-(ethoxycarbonyl)phenyl]-beta-alanine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(ethoxycarbonyl)phenyl]-beta-alanine(6959-76-8)
• EPA Substance Registry System: N-[4-(ethoxycarbonyl)phenyl]-beta-alanine(6959-76-8)

Safety Data

• Hazardous Substances Data: 6959-76-8(Hazardous Substances Data)

Upstream product

• 57-57-8 β-Propiolactone 
• 94-09-7 p-aminoethylbenzoate 

Downstream Products

• 51552-86-4 4-((2-carboxyethyl)amino)benzoic acid 
• 83704-89-6 N-(4-carbethoxycyclohexyl)-β-alanine 
• 79421-49-1 Ethyl N-(4-ethoxycarbonylphenyl)-3-aminopropanoate 
• 83704-96-5 1-<(2-amino-4-hydroxy-5-nitropyrimidin-6-yl)amino>-4--2,2-(ethylenedioxy)butane 
• 83710-11-6 4-[{2-[4-Oxo-2-(2,2,2-trifluoro-acetylamino)-3,4-dihydro-pteridin-6-yl]-ethyl}-(2,2,2-trifluoro-acetyl)-amino]-cyclohexanecarboxylic acid 
• 83704-97-6 1-<(2-amino-4-hydroxy-5-nitropyrimidin-6-yl)amino>-4-butan-2-one 
• 83704-98-7 4-[[4-(2,5-Diamino-6-oxo-1,6-dihydro-pyrimidin-4-ylamino)-3-oxo-butyl]-(2,2,2-trifluoro-acetyl)-amino]-cyclohexanecarboxylic acid ethyl ester 
• 83704-99-8 4-[[2-(2-Amino-4-oxo-3,4-dihydro-pteridin-6-yl)-ethyl]-(2,2,2-trifluoro-acetyl)-amino]-cyclohexanecarboxylic acid ethyl ester 
• 83704-88-5 1',2',3',4',5',6'-hexahydrohomofolic acid 
• 83704-94-3 1-azido-4--2,2-(ethylenedioxy)butane 
• 83704-93-2 1-azido-4-butane-2-one 

Relevant articles and documents

Design, synthesis and biological evaluation of novel pyrrolo[2,3-d]pyrimidine as tumor-targeting agents with selectivity for tumor uptake by high affinity folate receptors over the reduced folate carrier

Tumor-targeted 6-substituted pyrrolo[2,3-d]pyrimidine benzoyl compounds based on 2 were isosterically modified at the 4-carbon bridge by replacing the vicinal (C11) carbon by heteroatoms N (4), O (5) or S (6), or with an N-substituted formyl (7), trifluor