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Benzamide, N-[5-(cyanomethyl)-1,3,4-thiadiazol-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93355-73-8

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93355-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93355-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,5 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93355-73:
(7*9)+(6*3)+(5*3)+(4*5)+(3*5)+(2*7)+(1*3)=148
148 % 10 = 8
So 93355-73-8 is a valid CAS Registry Number.

93355-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[5-(cyanomethyl)-1,3,4-thiadiazol-2-yl]benzamide

1.2 Other means of identification

Product number -
Other names 2-benzoylamino-5-cyanomethyl-1,3,4-thiadiazole

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:93355-73-8 SDS

93355-73-8Relevant academic research and scientific papers

New approaches for the synthesis of 1,3,4-thiadiazole and 1,2,4-triazole derivatives with antimicrobial activity

Wardakhan, Wagnat W.,El-Sayed, Nahed N. E.

experimental part, p. 790 - 804 (2009/10/15)

The thiosemicarbazide derivatives 3a and 3b were cyclized in the presence of concentrated sulfuric acid to give the 5-cyanomethyl-1,3,4-thiadiazole derivatives 4a and 4b, respectively. The latter products were used for many heterocyclic transformations to

Hydrazones in heterocyclic synthesis; synthesis of 1,3,4-thiadiazole derivatives

Erian, Ayman Wahba,Manhi, Fatma Mohamed,Zayed, Salem El-Gohary,Ali, Fatma Ahmed,Elnagdi, Mohamed Hilmy

, p. 127 - 139 (2007/10/03)

A new synthesis of 1,3,4-thiadiazoles has been achieved. The reactivity of certain alkylheterocycles towards electrophilic reagents are reported.

STUDIES WITH POLYFUNCTIONALLY SUBSTITUTED HETEROAROMATICS: THE REACTIVITY OF ALKYLAZOLES TOWARDS ELECTROPHILIC REAGENTS

Zayed, Salem E.,Aziz, Suzan Ibrahim,Erian, Ayman Wahba,Mohareb, Rafat Milad,Elmaged, Eiman I. Abou,et al.

, p. 51 - 58 (2007/10/02)

Several new condensed thiadiazoles and thiazoles are synthesized.The reactivity of alkylazoles towards electrophilic reagents is reported.New synthesis of thienylthiadiazoles, thiadiazolopyridines and pyridazines could be achieved.Key words: Thiazoles and thiadiazoles, alkylheteroaromatics, and nucleophilic reagents and alkylazoles.

The Reaction of Isothiocyanates with 2-Cyanoethanoic Acid Hydrazide. A Novel Synthesis of 1,3,4-Thiadiazoles

Elmoghayar, Mohamed Rifaat Hamza,Abdalla, Sanaa Osman,Nasr, Mohamed Yousry Abdel-Samad

, p. 781 - 784 (2007/10/02)

Benzoyl and ethoxycarbonyl isothiocyanates reacted with 2-cyanoethanoic acid hydrazide 2 to afford 1-cyanoacetyl-4-substituted thiosemicarbazide (5a,b).Compound 5a afforded the pyrazolo-s-triazine derivative 6 on treatment with 5percent potassium h

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