Cas 1058739-49-3,tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate

1058739-49-3

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Basic information

Product Name: tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate
Synonyms: tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate
CAS NO:1058739-49-3
Molecular Formula:
Molecular Weight: 634.968
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: tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate(1058739-49-3)
EPA Substance Registry System: tert-butyl [[1-(5-chloro-1H-indol-2-carbonyl)-2,3-dihydro-1H-indol-5-yl]-(3,5-dichloro-phenylsulphonyl)-amino]-acetate(1058739-49-3)

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: 1058739-49-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1058739-49-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,3 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1058739-49:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*3)+(3*9)+(2*4)+(1*9)=183
183 % 10 = 3
So 1058739-49-3 is a valid CAS Registry Number.

1058739-49-3Upstream product

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1058739-49-3Relevant academic research and scientific papers

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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Page/Page column 78-79, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

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