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1,4-Dioxaspiro[4.5]decan-8-amine, N-methyl-N-(2-phenoxyethyl)-8-[3-(phenylmethoxy)phenyl]-, hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65620-07-7

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65620-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65620-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,2 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65620-07:
(7*6)+(6*5)+(5*6)+(4*2)+(3*0)+(2*0)+(1*7)=117
117 % 10 = 7
So 65620-07-7 is a valid CAS Registry Number.

65620-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(m-benzyloxyphenyl)-4-(N-methyl-N-β-phenoxyethylamino)cyclohexanone, ethylene ketal 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:65620-07-7 SDS

65620-07-7Upstream product

65620-07-7Downstream Products

65620-07-7Relevant academic research and scientific papers

4-Amino-4-phenylcyclohexanone ketal compositions and process of use

-

, (2008/06/13)

A class of new 4-amino-4-arylcyclohexanones, their ketals, and acid addition salts have been synthesized and found to be useful for relieving pain in animals. Their analgesic activity appears to be of high order, and in addition some exhibit narcotic antagonist activity that is useful in modifying the cardiovascular, respiratory, and behavioral depression caused by other analgesics. Several show mixed analgesic and narcotic antagonist activity. Preferred compounds of the class are 4-(m-hydroxyphenyl)-4-dimethylaminocyclohexanone ethylene ketal, and 4-(m-hydroxyphenyl)-4-(n-butylmethylamino)cyclohexanone ethylene ketal as free bases and as their hydrochloride salts. Processes for synthesis and intermediates are described. Unit dosage forms and therapeutic treatments are disclosed.

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