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7-Chlor-4-methoxy-1-indanon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34911-21-2

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34911-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34911-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,1 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34911-21:
(7*3)+(6*4)+(5*9)+(4*1)+(3*1)+(2*2)+(1*1)=102
102 % 10 = 2
So 34911-21-2 is a valid CAS Registry Number.

34911-21-2SDS

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 7-chloro-4-methoxy-indan-1-one

1.2 Other means of identification

Product number -
Other names 7-Chlor-4-methoxy-1-indanon

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:34911-21-2 SDS

34911-21-2Upstream product

34911-21-2Downstream Products

34911-21-2Relevant academic research and scientific papers

Analgesic and tranquilizing activity of 5,8 disubstituted 1 tetralone Mannich bases

Welch,Harbert,Sarges,Stratten,Weissman

, p. 699 - 705 (1977)

5,8-Disubstituted 1-tetralone Mannich bases represent semirigid variants of classical (i.e., chlorpromazine) neuroleptic agents. 8-Chloro-5-methoxy-2- morpholinomethyl-1-tetralone exhibits neuroleptic potency in the thiothixene range in animal models. Of greater potential interest, however, is the analgesic potency of the 8-chloro-5-methoxy-2-pyrrolidinomethyl analogue which was in the morphine range. This compound did not induce tolerance nor was its activity reversed by naloxone. Structure-activity relationships of the series are discussed.

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