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115732-15-5

115732-15-5

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115732-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115732-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,3 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115732-15:
(8*1)+(7*1)+(6*5)+(5*7)+(4*3)+(3*2)+(2*1)+(1*5)=105
105 % 10 = 5
So 115732-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO3/c19-16(12-6-2-1-3-7-12)18-11-14-9-5-4-8-13(14)10-15(18)17(20)21/h1-9,15H,10-11H2,(H,20,21)

115732-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzoyl-L-3-carboxy-1,2,3,4-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 2-BENZOYL-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID

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:115732-15-5 SDS

115732-15-5Downstream Products

115732-15-5Relevant articles and documents

N-Acylphenylalanines and Related Compounds. A New Class of Oral Hypoglycemic Agents

Shinkai, Hisashi,Toi, Koji,Kumashiro, Izumi,Seto, Yoshiko,Fukuma, Mariko,et al.

, p. 2092 - 2097 (2007/10/02)

N-Benzoyl-DL-phenylalanine (1) was found to possess hypoglycemic activity.A series of the analogues of compound 1 were prepared and evaluated for their blood glucose lowering activity.Both the steric effects of the phenylalanine moiety and the effects of variations in the acyl moiety were investigated.This study elucidated some of the structure-activity relationships and led to the development of N-(4-ethylbenzoyl)-D-phenylalanine (34), which was 50 times more potent than the initial compound 1.

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