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78760-14-2

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  • 1H-Tetrazole, 5-(5-chloropentyl)-1-cyclohexyl- Manufacturer Factory CAS 78760-14-2

    Cas No: 78760-14-2

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78760-14-2 Usage

Chemical structure

Contains a tetrazole ring and a cyclohexyl group.

Usage

Utilized in the synthesis of pharmaceuticals and in chemical research.

Potential applications

May be involved in the development of new drugs and the study of tetrazole chemistry.

Safety precautions

Proper handling and storage procedures should be followed to ensure safety and prevent adverse effects.

Physical properties

Not provided in the material.

Chemical properties

Not provided in the material.

Check Digit Verification of cas no

The CAS Registry Mumber 78760-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,6 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78760-14:
(7*7)+(6*8)+(5*7)+(4*6)+(3*0)+(2*1)+(1*4)=162
162 % 10 = 2
So 78760-14-2 is a valid CAS Registry Number.

78760-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(5-chloropentyl)-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:78760-14-2 SDS

78760-14-2Relevant articles and documents

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 (1983)

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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