Cas 264188-57-0,2-(3,4-dimethoxy-phenyl)-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-propionic acid ethyl ester

264188-57-0

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Basic information

Product Name: 2-(3,4-dimethoxy-phenyl)-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-propionic acid ethyl ester
Synonyms:
CAS NO:264188-57-0
Molecular Formula:
Molecular Weight: 454.48
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-(3,4-dimethoxy-phenyl)-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,4-dimethoxy-phenyl)-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-propionic acid ethyl ester(264188-57-0)
EPA Substance Registry System: 2-(3,4-dimethoxy-phenyl)-3-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-propionic acid ethyl ester(264188-57-0)

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: 264188-57-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 264188-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,1,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 264188-57:
(8*2)+(7*6)+(6*4)+(5*1)+(4*8)+(3*8)+(2*5)+(1*7)=160
160 % 10 = 0
So 264188-57-0 is a valid CAS Registry Number.

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264188-57-0Relevant 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 (2007/10/03)

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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