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Benzeneacetamide, N-[5-[(phenylmethyl)amino]-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.

109853-22-7

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109853-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109853-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109853-22:
(8*1)+(7*0)+(6*9)+(5*8)+(4*5)+(3*3)+(2*2)+(1*2)=137
137 % 10 = 7
So 109853-22-7 is a valid CAS Registry Number.

109853-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names N-[5-(benzylamino)-1,3,4-thiadiazol-2-yl]phenylacetamide

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:109853-22-7 SDS

109853-22-7Downstream Products

109853-22-7Relevant academic research and scientific papers

Versatile strategies for the solid phase synthesis of small heterocyclic scaffolds: [1,3,4]-Thiadiazoles and [1,3,4]-oxadiazoles

Severinsen, Rune,Kilburn, John Paul,Lau, Jesper F.

, p. 5565 - 5575 (2007/10/03)

New robust protocols for the solid phase synthesis of 5-alkylthio-, 5-alkyl/aryl-, and 5-acylamino-2-alkylamino-[1,3,4]-thiadiazoles are described based on a common resin bound thiosemicarbazide. A protocol for the solid phase synthesis of 2-alkyl/aryl-amino-5-alkylamino-[1,3,4]-oxadiazoles from a resin bound semicarbazide is likewise reported. The protocols have been verified by the preparation of four small libraries that all gave products in good to excellent yields and purity.

1,3,4-THIADIAZOLES USEFUL FOR THE TREATMENT OF CMV INFECTIONS

-

, (2008/06/13)

The present invention presents novel 1,3,4-thiadiazole derivatives of formula I which have useful antiviral activity against herpes virus, cytomegalovirus (CMV).

A new route to 1,2,4-triazoles and 1,3,4-thiadiazoles from 1-acylbithiourea

Okawara,Tateyama,Yamasaki,Furukawa

, p. 1071 - 1075 (2007/10/02)

The intramolecular cyclization of 1-acylbithiourea 1 gave 1,2,4-triazole 2 and 1,3,4-thiadiazole 3. The reaction of 1 with p-toluenesulfonyl chloride in the presence of triethylamine afforded 3. Treatment of 1 with methyl iodide in the absence of any base yielded 2-methylthio-1,3,4-thiadiazole 10 and 2-imino-1,3,4-thiadiazoline 12.

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