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68723-63-7

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68723-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68723-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,2 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68723-63:
(7*6)+(6*8)+(5*7)+(4*2)+(3*3)+(2*6)+(1*3)=157
157 % 10 = 7
So 68723-63-7 is a valid CAS Registry Number.

68723-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dithiophen-2-yl-1,2,4-selenadiazole

1.2 Other means of identification

Product number -
Other names 3,5-Bis-<2>thienyl-1,2,4-selenazol

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:68723-63-7 SDS

68723-63-7Downstream Products

68723-63-7Relevant articles and documents

The facile and efficient organocatalytic platform for accessing 1,2,4-selenadiazoles and thiadiazoles under aerobic conditions

Putta, V.P. Rama Kishore,Gujjarappa, Raghuram,Vodnala, Nagaraju,Gupta, Richa,Pujar, Prasad P.,Malakar, Chandi C.

supporting information, p. 904 - 908 (2018/02/06)

The first organocatalytic approach towards synthesis of rarely explored 1,2,4-selenadiazole and thiadiazole scaffolds have been devised using corresponding carboxamides as substrates. The transformations were realized using two distinct conditions in the presence of catalytic vitamin B3 or thiourea under aerobic conditions. Developed methods overcome the associated limitations of previous reported approaches and the desired products were obtained in high yields and selectivity without the formation of toxic side-products.

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