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N,N-bis(acetylthiomethyl)-p-chloroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127099-06-3

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127099-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127099-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127099-06:
(8*1)+(7*2)+(6*7)+(5*0)+(4*9)+(3*9)+(2*0)+(1*6)=133
133 % 10 = 3
So 127099-06-3 is a valid CAS Registry Number.

127099-06-3Relevant academic research and scientific papers

Nickel(II)-Nickel(II) Azadithiolates: Synthesis, Structural Characterization, and Electrocatalytic H2Production

Song, Li-Cheng,Liu, Wen-Bo,Liu, Bei-Bei

, p. 1431 - 1439 (2020)

Azadithiolato-bridged dinuclear Ni2 complexes with the general formula [(η5-C5H5)Ni{(μ-SCH2)2NC6H4R-4}Ni(diphos)]BF4 (8-11, R = H, Cl, MeO; diphos = dppv, dppe) have been prepared by a well-designed synthetic method including the following three separate

N-Substituted Derivatives of the Azadithiolate Cofactor from the [FeFe] Hydrogenases: Stability and Complexation

Angamuthu, Raja,Chen, Chi-Shian,Cochrane, Tyler R.,Gray, Danielle L.,Schilter, David,Ulloa, Olbelina A.,Rauchfuss, Thomas B.

, p. 5717 - 5724 (2015)

Experiments are described that probe the stability of N-substituted derivatives of the azadithiolate cofactor recently confirmed in the [FeFe] hydrogenases (Berggren, G., et al. Nature 2013, 499, 66). Acid-catalyzed hydrolysis of bis(thioester) BnN(CHsub

Syntheses of optically active γ-ketothiols and the esters by lipase-catalyzed hydrolysis via α-acetylthiomethylation of ketones

Izawa, Tomohiko,Terao, Yoshiyasu,Suzuki, Kunio

, p. 2645 - 2648 (2007/10/03)

The α-acetylthiomethylation of ketones was achieved by the reaction of ketones or the enamines with N,N-bis-(acetylthiomethyl)-p-chloroaniline in the presence of trifluoroacetic acid. The resulting thiolesters were hydrolyzed enantioselectively by catalys

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