Cas 97529-58-3,2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester

97529-58-3

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Basic information

Product Name: 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester
Synonyms: 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester
CAS NO:97529-58-3
Molecular Formula:
Molecular Weight: 409.398
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: 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(97529-58-3)
EPA Substance Registry System: 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(97529-58-3)

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: 97529-58-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97529-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,2 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97529-58:
(7*9)+(6*7)+(5*5)+(4*2)+(3*9)+(2*5)+(1*8)=183
183 % 10 = 3
So 97529-58-3 is a valid CAS Registry Number.

97529-58-3Upstream product

97529-58-3Downstream Products

97500-82-8 2-[2-(5-Nitro-1H-indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid

97529-58-3Relevant academic research and scientific papers

N-(indole-3-ylglyoxyl) aminoacid derivatives. Preparation and pharmacological properties

Da Settimo,Primofiore,Marini,et al.

, p. 507 - 511 (2007/10/02)

The authors describe the synthesis of several N-(indole-3-ylglyoxyl) aminoacid derivatives. The target compounds were prepared starting from substituted indoleglyoxyl chlorides and some aminoacid esters. Some of them were tested for their antiinflammatory

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