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114751-76-7

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114751-76-7 Usage

Type

Organic compound

Usage

Commonly used in the pharmaceutical industry for drug synthesis

Biological activities

Antifungal, antibacterial, antitumor properties

Application

Used as a building block in medicinal chemistry for pharmaceutical development

Potential use

Investigated for use in organic semiconductor materials

Unique properties

Nitrogen-containing heterocyclic compound

Check Digit Verification of cas no

The CAS Registry Mumber 114751-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114751-76:
(8*1)+(7*1)+(6*4)+(5*7)+(4*5)+(3*1)+(2*7)+(1*6)=117
117 % 10 = 7
So 114751-76-7 is a valid CAS Registry Number.

114751-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-Pentyl-phenyl)-[1,3,4]thiadiazol-2-ylamine

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:114751-76-7 SDS

114751-76-7Relevant articles and documents

Synthesis of N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol- 2(3H)-yl)acetamide derivatives promoted by carbodiimide condensation

Yu, Peng,Hu, Jun,Wan, Rong,Li, Xi,Zheng, Shanlong,Xu, Yanhua

, p. 347 - 350 (2014/07/08)

Novel N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol-2(3H)-yl) acetamide derivatives were prepared by 1-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride and N-hydroxybenzotrizole condensation catalysis in a convenient and fast method

LIQUID-CRYSTALLINE IMIDAZO-1,3,4-THIADIAZOLES. I. SYNTHESIS OF 2,6-DISUBSTITUTED IMIDAZO-1,3,4-THIADIAZOLES AND THEIR MESOMORPHOUS AND SPECTRAL CHARACTERISTICS

Torgova, S. I.,Abolin, A. G.,Karamysheva, L. A.,Ivashchenko, A. V.

, p. 172 - 178 (2007/10/02)

Derivatives of imidazo-1,3,4-thiadiazole possessing a wide temperature range of smectic mesophase were obtained.The introduction of the cyclohexane fragment into the imidazole part of the molecule promotes the appearance of the nematic mesophase.The structure of the new mesogens and of the intermediates in their synthesis were confirmed by the data from IR and (13)C and (1)H NMR spectroscopy.

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