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86717-05-7

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86717-05-7 Usage

Type of Compound

Potent and selective β3-adrenoceptor agonist

Application

Used in pharmacological research to study the function of β3-adrenoceptors

β3-adrenoceptors role

Involved in the regulation of metabolism and energy expenditure

Effectiveness

Promotes lipolysis, increases thermogenesis, and improves insulin sensitivity in animal studies

Potential Treatment

Obesity, type 2 diabetes, and other metabolic disorders

Unique Structure

Contributes to its pharmacological properties

Value

Serves as a valuable tool for understanding the role of β3-adrenoceptors in health and disease

Check Digit Verification of cas no

The CAS Registry Mumber 86717-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86717-05:
(7*8)+(6*6)+(5*7)+(4*1)+(3*7)+(2*0)+(1*5)=157
157 % 10 = 7
So 86717-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H20ClN5OS2/c21-16-6-2-4-8-18(16)23-11-14(27)12-28-20-26-25-19(29-20)24-10-13-9-22-17-7-3-1-5-15(13)17/h1-9,14,22-23,27H,10-12H2,(H,24,25)

86717-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroanilino)-3-[[5-(1H-indol-3-ylmethylamino)-1,3,4-thiadiazol-2-yl]sulfanyl]propan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Propanol,1-((2-chlorophenyl)amino)-3-((5-((1H-indol-3-ylmethyl)amino)-1,3,4-thiadiazol-2-yl)thio)

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:86717-05-7 SDS

86717-05-7Downstream Products

86717-05-7Relevant articles and documents

Anti-inflammatory, antiproteolytic and analgesic activities of some new thiadiazolyl indoles

Tandon,Barthwal,Bhalla,Tandon,Bhargava

, p. 493 - 499 (2007/10/02)

3-[(2-aminomethyl)-5-mercapto-1,3,4-thiadiazolyl]indole (1), obtained by Mannich condensation of 2-amino-5-mercapto-1,3,4-thiadiazole with indole and formaldehyde, was subjected to mercaptoetherification with epichlorohydrin to yield 3-[(2-aminoethyl)-5-(

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