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5-(3-Chloropropyl)-1-cyclohexyltetrazole is an organic compound characterized by its unique molecular structure, which features a cyclohexyl group and a tetrazole ring. 5-(3-Chloropropyl)-1-cyclohexyltetrazole is known for its reactivity and potential applications in various chemical and pharmaceutical processes.

73963-29-8

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73963-29-8 Usage

Uses

Used in Pharmaceutical Industry:
5-(3-Chloropropyl)-1-cyclohexyltetrazole is used as a reactant for the synthesis of 5-(3-aryloxypropyl)-1-cyclohexyltetrazole derivatives. These derivatives exhibit inhibitory activity towards collagenand adenosinediphosphate-induced aggregation of rabbit blood platelets in vitro. This property makes them valuable in the development of medications aimed at treating conditions related to blood clotting and platelet aggregation, such as thrombosis and cardiovascular diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 73963-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73963-29:
(7*7)+(6*3)+(5*9)+(4*6)+(3*3)+(2*2)+(1*9)=158
158 % 10 = 8
So 73963-29-8 is a valid CAS Registry Number.

73963-29-8SDS

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 5-(3-chloropropyl)-1-cyclohexyltetrazole

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:73963-29-8 SDS

73963-29-8Relevant academic research and scientific papers

Studies on 2-oxoquinoline derivatives as blood platelet aggregation inhibitors. II. 6-[3-(1-Cyclohexyl-5-tetrazolyl)propoxy]-1,2-dihydro-2-oxoquinoline and related compounds

Nishi,Tabusa,Tanaka,Shimizu,Kanbe,Kimura,Nakagawa

, p. 1151 - 1157 (2007/10/02)

A series of ω-(1-substituted-5-tetrazolylalkoxy)-2-oxoquinolines was synthesized and tested for inhibitory activity towards collagen- and adenosine diphosphate (ADP)-induced aggregation of rabbit blood platelets in vitro. These compounds were prepared by the reaction of 1-substituted-5-(ω-chloroalkyl)-tetrazoles and hydroxy-2-oxoquinolines in the presence of a base. Among them, 6-[3-(1-cyclohexyl-5-tetrazolyl)propoxy]-1,2-dihydro-2-oxoquinoline (IVb) was found to have the most potent inhibitory activity. The structure-activity relationships are discussed.

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