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methyl 6-(4-methoxybenzyl)-1,5,5-trimethyl-4-oxopiperidine-3-carboxylate hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31648-24-5

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31648-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31648-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,4 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31648-24:
(7*3)+(6*1)+(5*6)+(4*4)+(3*8)+(2*2)+(1*4)=105
105 % 10 = 5
So 31648-24-5 is a valid CAS Registry Number.

31648-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(p-methoxybenzyl)-4-oxo-1,3,3-trimethyl-5-piperidine-carboxylate hydrochloride

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:31648-24-5 SDS

31648-24-5Upstream product

31648-24-5Downstream Products

31648-24-5Relevant academic research and scientific papers

2-Benzyl-4-piperidones useful as intermediates in the production of 6,7-benzomorphan derivatives

-

, (2008/06/13)

6,7-BENZOMORPHAN DERIVATIVES HAVING ANALGESIC AND MORPHINE-ANTAGONISTIC PROPERTIES ARE OF THE FORMULA STR1 in which the substituents R are either lower alkyl groups or groups which, together with the carbon atom to which they are bonded, form a cycloaliphatic ring, and the substituents R1, R2 and R 3 may or may not be made and, if made, R1 represents either a hydrogen atom or an alkyl, haloalkyl, alkenyl, alkinyl, aralkyl, cycloalkenyl, cycloalkylalkyl, cycloalkenylalkyl or cycloalkylidine-alkyl group, R 2 is an alkyl, aryl, heteroaryl or aralkyl group, and R 3 is a hydrogen atom or an hydroxy, alkoxy, alkoxy-alkoxy or acyloxy group. Such 6,7-benzomorphans may be in the form of their optically active enantiomers and/or their therapeutically acceptable salts. There are also disclosed methods for producing such 6,7-benzomorphan derivatives, and intermediates useful in such production.

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