Cas 129585-46-2,5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

129585-46-2

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Basic information

Product Name: 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester
Synonyms: 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester
CAS NO:129585-46-2
Molecular Formula:
Molecular Weight: 354.836
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: 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester(129585-46-2)
EPA Substance Registry System: 5-(2-Amino-phenyl)-4-chloro-2-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester(129585-46-2)

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: 129585-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129585-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,8 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129585-46:
(8*1)+(7*2)+(6*9)+(5*5)+(4*8)+(3*5)+(2*4)+(1*6)=162
162 % 10 = 2
So 129585-46-2 is a valid CAS Registry Number.

129585-46-2Upstream product

129585-46-2Downstream Products

82168-92-1 1-Ethoxycarbonyl-2-methyl-3-phenylpyrrolo<3,2-c>cinnoline

129585-46-2Relevant academic research and scientific papers

Polycondensed Nitrogen Heterocycles. Part 23. Pyrrolocinnolines by a Japp-Klingemann Type Reaction

Cirrincione, Girolamo,Almerico, Anna Maria,Aiello, Enrico,Dattolo, Gaetano

, p. 983 - 985 (2007/10/02)

Pyrrolocinnoline derivatives were obtained by an unusual Japp-Klingemann reaction involving an intramolecular azadehalogenation on the pyrrole nucleus.Such an azadehalogenation represents the first example of Japp-Klingemann reaction in which the e

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