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131028-34-7

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131028-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131028-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,2 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131028-34:
(8*1)+(7*3)+(6*1)+(5*0)+(4*2)+(3*8)+(2*3)+(1*4)=77
77 % 10 = 7
So 131028-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H26N2O2/c1-25-21(24)20-9-5-8-18(16-20)10-11-22-12-14-23(15-13-22)17-19-6-3-2-4-7-19/h2-9,16H,10-15,17H2,1H3

131028-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[2-(4-benzylpiperazin-1-yl)ethyl]benzoate

1.2 Other means of identification

Product number -
Other names -

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:131028-34-7 SDS

131028-34-7Downstream Products

131028-34-7Relevant articles and documents

POTENTIAL NOOTROPIC AGENTS: SYNTHESIS OF A SERIES OF (2-OXO-1-PYRROLIDINYL)ACETIC ACID PIPERAZIDES

Valenta, Vladimir,Sindelar, Karel,Holubek, Jiri,Ryska, Miroslav

, p. 1613 - 1629 (2007/10/02)

The title compounds VI-XXIII were prepared by heating ethyl (2-oxo-1-pyrrolidinyl)acetate (II) with a series of N-monosubstituted piperazines.The propionamides XXVI and XXX were obtained by reactions of the acid chlorides IV and XXXIII with 3-(1-piperazinyl)propionamide.Compounds VI (VUFB-13 763) and VIII (VUFB-14 745) proved more active than piracetam (I) by their antiamnestic effects in rats by antagonising the brain demaging effects of cycloheximide in infantile rats, and by their potentation of the effects of anticolvunsant agents.

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