Cas 293735-38-3,1-(<i>tert</i>-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid 4-nitro-phenyl ester

293735-38-3

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Basic information

Product Name: 1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid 4-nitro-phenyl ester
Synonyms:
CAS NO:293735-38-3
Molecular Formula:
Molecular Weight: 483.478
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: 1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid 4-nitro-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid 4-nitro-phenyl ester(293735-38-3)
EPA Substance Registry System: 1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid 4-nitro-phenyl ester(293735-38-3)

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: 293735-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 293735-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,7,3 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 293735-38:
(8*2)+(7*9)+(6*3)+(5*7)+(4*3)+(3*5)+(2*3)+(1*8)=173
173 % 10 = 3
So 293735-38-3 is a valid CAS Registry Number.

293735-38-3Upstream product

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293735-38-3Relevant academic research and scientific papers

1-Aminomethylisoquinoline-4-carboxylates as novel dipeptidylpeptidase IV inhibitors

Coppola, Gary M.,Zhang, Y. Larry,Schuster, Herbert F.,Russell, Mary E.,Hughes, Thomas E.

, p. 1555 - 1558 (2000)

Structure-activity relationship within a series of 1-aminoalkylisoquinoline-4-carboxylates as inhibitors of DDP-IV is described. A primary aminomethyl group is required to maintain biological activity. Substitution of the isoquinoline at the 6- and 8-positions with methoxy groups increases potency to 53 times that of the lead compound SDZ 029-576. (C) 2000 Elsevier Science Ltd. All rights reserved.

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