Cas 867349-73-3,3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester

867349-73-3

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Basic information

Product Name: 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester
Synonyms: 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester
CAS NO:867349-73-3
Molecular Formula:
Molecular Weight: 319.428
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester(867349-73-3)
EPA Substance Registry System: 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulfanyl)-propionic acid methyl ester(867349-73-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 867349-73-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867349-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,3,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 867349-73:
(8*8)+(7*6)+(6*7)+(5*3)+(4*4)+(3*9)+(2*7)+(1*3)=223
223 % 10 = 3
So 867349-73-3 is a valid CAS Registry Number.

867349-73-3Upstream product

867349-72-2 3-(1-benzyl-2-ethyl-4-nitro-1H-imidazol-5-ylsulfanyl)propionic acid methyl ester

867349-73-3Downstream Products

867349-73-3Relevant academic research and scientific papers

Nitroimidazoles, part 1. An unexpected reactivity during the cyclization of 3-(4-amino-1-benzyl-2-ethyl-1H-imidazol-5-ylsulphanyl)-propionic acid methyl ester

Al-Soud, Yaseen A.,Al-Masoudi, Najim A.

, p. 2259 - 2264 (2007/10/03)

Nucleophilic substitution of the 5-bromo group in 1 by methyl 3-mercaptopropionate gave the 5-alkyl-mercapto derivative 2. Reduction of 2 with H2/Pd led to the amine 3, meanwhile reduction with Fe/HOAc afforded the 5-acetamido derivative 4 and

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