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132553-86-7

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132553-86-7 Usage

Uses

Anti-anxiety agent.

Check Digit Verification of cas no

The CAS Registry Mumber 132553-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,5 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132553-86:
(8*1)+(7*3)+(6*2)+(5*5)+(4*5)+(3*3)+(2*8)+(1*6)=117
117 % 10 = 7
So 132553-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H25NO/c22-20(18-9-5-2-6-10-18)19-12-15-21(16-13-19)14-11-17-7-3-1-4-8-17/h1-10,19-20,22H,11-16H2

132553-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Glemanserin

1.2 Other means of identification

Product number -
Other names ALPHA-PHENYL-1-(2-PHENYLETHYL)-4-PIPERIDINEMETHANOL

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:132553-86-7 SDS

132553-86-7Relevant articles and documents

An efficient synthesis of N-alkyl-4-substituted 3H-pyridine-2,6-dione. Synthesis of isoguvacine and MDL-11,939

Chang, Meng-Yang,Chen, Shui-Tein,Chang, Nein-Chen

, p. 2321 - 2334 (2007/10/03)

An efficient route towards the synthesis of N-alkyl-4-substituted 3H-pyridine-2,6-dione using various N-alkyl-α-sulfonylacetamides and two α,β-unsaturated esters as starting materials is described. Isoguvacine and MDL-11,939 with have potential biological activities were synthesized via this strategy.

N-ARALKYL PIPERIDINE METHANOL DERIVATIVES AND THE USES THEREOF

-

, (2008/06/13)

This invention relates to a new class of compounds having important biochemical and pharmacological properties. More particularly, this invention relates to N-aralkyl piperidinemethanol derivatives which are potent and selective inhibitors of the binding

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