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138117-79-0

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138117-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138117-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,1 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138117-79:
(8*1)+(7*3)+(6*8)+(5*1)+(4*1)+(3*7)+(2*7)+(1*9)=130
130 % 10 = 0
So 138117-79-0 is a valid CAS Registry Number.

138117-79-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[3-(1,6-dihydro-6-oxo-9H-purin-9-yl)-1-oxopropyl]amino]benzoic acid,ethyl ester

1.2 Other means of identification

Product number -
Other names 4-[[3-(1,6-dihydro-6-oxo-9H-purin-9-yl)-1-oxopropyl-] amino] benzoic acid, ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:138117-79-0 SDS

138117-79-0Downstream Products

138117-79-0Relevant articles and documents

A new method for synthesis and angiogenic evaluation of leteprinim potassium and its novel analogs

Sakakibara, Norikazu,Tsukamoto, Ikuko,Isono, Yohei,Takata, Maki,Konishi, Ryoji,Kato, Yoshihisa,Maruyama, Tokumi

, p. 2369 - 2384 (2013/11/19)

We developed a novel pathway for the successful synthesis of leteprinim potassium 1, which is one of the candidate substances for treating Alzheimer's disease, and subsequently synthesized 4 types of corresponding novel derivatives 2-5 that have hypoxanthine or 2-chloro-6-aminopurine as the nucleobase. We then determined the angiogenic activity of these compounds by using human umbilical vein endothelial cells. Compounds 1-4 showed no angiogenic potencies judging from statistical analysis, student's t-test.

9-substituted hypoxanthine bi-functional compounds and their neuroimmunological methods of use

-

, (2008/06/13)

Novel bi-functional pharmaceutical compounds, particularly novel 9-substituted hypoxanthines of the general formula: STR1 where R is a neurologically active moiety, are described as pharmaceutical agents for treating neuroimmunologic disorders in mammals. Novel methods for the utilization of these compounds are also disclosed. These compounds exhibit uniquely dose-dependent, synergistic biological properties and are particularly useful for treating interrelated physiological systems.

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