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1,3,4-Thiadiazol-2-amine, 5-(3-chlorobenzo[b]thien-2-yl)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142137-79-9

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142137-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142137-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,3 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142137-79:
(8*1)+(7*4)+(6*2)+(5*1)+(4*3)+(3*7)+(2*7)+(1*9)=109
109 % 10 = 9
So 142137-79-9 is a valid CAS Registry Number.

142137-79-9Downstream Products

142137-79-9Relevant academic research and scientific papers

In silico investigation applied in physical, chemical properties and vibrational analysis of 1.3.4-thiadiazole derivatives

AOUMEUR, Nabila,TCHOUAR, Noureddine,BELAIDI, Salah,HARKATI, Dalal,BELAIDI, Houmam,ROUANE, Abderrahmane

, p. 935 - 948 (2021/02/05)

The equilibrium geometries of 1,3,4-thiadiazole derivatives have been determined and analyzed at DFT level employing B3LYP/6-31G(d) basis set. The molecular electrostatic potential surface (MESP) that reveals centers of reactivity of the molecule and subs

In silico investigation applied in physical, chemical properties and vibrational analysis of 1.3.4-thiadiazole derivatives

Aoumeur, Nabila,Belaidi, Houmam,Belaidi, Salah,Harkati, Dalal,Rouane, Abderrahmane,Tchouar, Noureddine

, p. 935 - 948 (2020/06/27)

The equilibrium geometries of 1,3,4-thiadiazole derivatives have been determined and analyzed at DFT level employing B3LYP/6-31G(d) basis set. The molecular electrostatic potential surface (MESP) that reveals centers of reactivity of the molecule and subs

Synthesis, antimicrobial, and anthelmintic activities of some new 3-chlorobenzothiophene-2-carbonylchloride derivatives

Naganagowda, Gadada,Padmashali, Basavaraj

experimental part, p. 1691 - 1700 (2010/10/01)

3-Chlorobenzothiophene-2-carbonylchloride 1 was prepared from cinnamic acid and then converted into the acid hydrazide 2. Reaction of 3-chloro-1- benzothiophene-2-carbohydrazide 2 with the appropriate isothiocyanate yielded the substituted thiosemicarbazi

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