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Tetrazolo[1,5-d][1,2,4]triazin-8(7H)-one, 5-methyl-7-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61145-30-0

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61145-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61145-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,4 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61145-30:
(7*6)+(6*1)+(5*1)+(4*4)+(3*5)+(2*3)+(1*0)=90
90 % 10 = 0
So 61145-30-0 is a valid CAS Registry Number.

61145-30-0SDS

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 5-methyl-7-phenyltetrazolo[1,5-d][1,2,4]triazin-8-one

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:61145-30-0 SDS

61145-30-0Downstream Products

61145-30-0Relevant academic research and scientific papers

A Synthetic Route Toward Tetrazoles: The Thermolysis of Geminal Diazides

Holzschneider, Kristina,Kirsch, Stefan F.,Mohr, Fabian,Tong, My Linh

, (2019/08/21)

A new synthetic route toward the tetrazole core is described, which is based on a general fragmentation pattern that was found in a range of compounds featuring geminal diazido units. Through a simple two-step procedure, the synthesis of structurally diverse target compounds containing a tetrazole, such as tetrazoloquinoxalinones, benzoylaryltetrazoles, tetrazolotriazinones, and tetrazoloazepinones, was easily accomplished, starting from broadly accessible substrates (i.e., oxindoles, diarylethanones, pyrazolones, and phenanthrols). The initial oxidative diazidation reaction with iodine and sodium azide under mild conditions is followed by the thermal fragmentation under microwave irradiation, leading to the tetrazole products. Noteworthy, an experimental solution is presented in which the potentially hazardous diazide intermediates are not isolated and the concentration of crude reaction mixtures containing diazides is not required to achieve the tetrazoles in good yields.

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