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1H-Indene, 4-(chloromethyl)-2,3-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65898-31-9

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65898-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65898-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65898-31:
(7*6)+(6*5)+(5*8)+(4*9)+(3*8)+(2*3)+(1*1)=179
179 % 10 = 9
So 65898-31-9 is a valid CAS Registry Number.

65898-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloromethylindane

1.2 Other means of identification

Product number -
Other names 4-Chloromethylindan

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:65898-31-9 SDS

65898-31-9Downstream Products

65898-31-9Relevant academic research and scientific papers

SYNTHESIS OF TRICYCLIC BENZAZEPINES AND THEIR DOPAMINE D1- AND D2-AFFINITY

Horn Jensen, Eva,Nielsen, Per Halfdan

, p. 2441 - 2458 (2007/10/03)

A new group of angular 8,9-annelated 3-benzazepines has been found to be potent and selective dopamine D1-receptor antagonists of interest as possible pharmaceuticals in the treatment of schizophrenia.The synthesis of three new conformationally constrained representatives of this group of benzazepines is described and their affinity to the D1-receptor evaluated.Although none of these proved superior to the previously examined compounds, useful information on the receptor binding site was obtained.

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