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2-Naphthalenecarbothioamide, 1,2,3,4-tetrahydro-N-(4-methylphenyl)-1-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125341-79-9

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125341-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125341-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,4 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125341-79:
(8*1)+(7*2)+(6*5)+(5*3)+(4*4)+(3*1)+(2*7)+(1*9)=109
109 % 10 = 9
So 125341-79-9 is a valid CAS Registry Number.

125341-79-9Relevant academic research and scientific papers

Enantioselective Construction of Polyfunctionalized Spiroannulated Dihydrothiophenes via a Formal Thio [3+2] Cyclization

Zeng, Xue-Mei,Meng, Chang-Yu,Bao, Jia-Xin,Xu, Dong-Cheng,Xie, Jian-Wu,Zhu, Wei-Dong

, p. 11521 - 11528 (2015)

A formal thio [3+2] cyclization catalyzed by Takemoto's organocatalyst has been reported for the construction of optically active spiroannulated dihydrothiophenes in high yields with excellent regio-, chemo-, diastereo-, and enantioselectivities.

2-Aryl-3-phenylamino-4,5-dihydro-2h-benz[g]indazoles with analgesic activity

Schenone, Silvia,Bruno, Olga,Ranise, Angelo,Brullo, Chiara,Bondavalli, Francesco,Filippelli, Walter,Mazzeo, Filomena,Capuano, Annalisa,Falcone, Giuseppe

, p. 845 - 849 (2007/10/03)

A series of 2-aryl-3-phenylamino-4,5-dihydro-2H-benz[g]indazoles was synthesized and tested for antiarrhythmic, local anaesthetic and analgesic activity. The title compounds showed a good antinociceptive activity.

Phase Transfer Catalysed Alkylation of Enamines of β-Keto Carbothionic Acid Anilides with Dihalogenoalkanes: Synthesis of Cyclic S,N-Acetals of α-Oxo Ketene

Bogdanowicz-Szwed, Krystyna,Kozicka, Michalina,Lipowska, Malgorzata

, p. 231 - 242 (2007/10/02)

Alkylation of 2-morpholino-cycloalken-1-carbothionic acid anilides 1 and 2 with 1,3-dibromopropane in a two-phase system leads to 1-morpholino-cycloalken-3-aryl-tetrahydro-1,3-thiazine-2-ylidene 3 and 4.Reactions of 2-morpholino-cyclopenten-1-carbothionic

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