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53716-48-6

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53716-48-6 Usage

Uses

Analgesic.

Check Digit Verification of cas no

The CAS Registry Mumber 53716-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,1 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53716-48:
(7*5)+(6*3)+(5*7)+(4*1)+(3*6)+(2*4)+(1*8)=126
126 % 10 = 6
So 53716-48-6 is a valid CAS Registry Number.

53716-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-[1-(dimethylamino)propan-2-yl]-2-phenylcyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-(2-Dimethylamino-1-methylethyl)-2-phenylcyclohexyl acetate

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:53716-48-6 SDS

53716-48-6Upstream product

53716-48-6Downstream Products

53716-48-6Relevant articles and documents

1-(Amino-alkyl)-2-aryl-cyclohexane alcohols and esters

-

, (2008/06/13)

Analgesics, local anesthetics, and antiarrhythmics which are 1-(amino-alkyl)-2-aryl-cyclohexane alcohols and esters having the structure SPC1 Wherein R1 is hydrogen or alkanoyl; R2 and R3 individually are hydrogen, lower alkyl, or lower alkenyl, or R2 and R3 together with the nitrogen to which they are attached form a morpholine radical, a piperazine radical or a carbocyclic ring; R4 is hydrogen or lower alkyl; R5 and R6 individually are hydrogen, lower alkyl, hydroxyl or lower alkoxy; and the pharmaceutically acceptable acid addition and quaternary salts thereof, as well as stereoisomers and optical isomers thereof. This invention relates also to processes for making and using the foregoing compounds.

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