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N-(Mesitylsulfonyl)carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56830-76-3

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56830-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56830-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,3 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56830-76:
(7*5)+(6*6)+(5*8)+(4*3)+(3*0)+(2*7)+(1*6)=143
143 % 10 = 3
So 56830-76-3 is a valid CAS Registry Number.

56830-76-3Relevant academic research and scientific papers

Substituted heteroaryl compounds and compositions and uses thereof (by machine translation)

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Paragraph 1059; 1061;1062; 1063, (2019/06/07)

The invention discloses substituted heteroaryl compounds and compositions thereof and their use. The compounds of formula (I) compound or type shown in (I) a compound represented by stereo isomers, tautomers, nitrogen oxide, solvate, metabolite, pharmaceutically acceptable salt or its prodrug. The invention also provides a pharmaceutical composition, the compounds and pharmaceutical compositions can be regulated protein kinase, particularly Aurora kinase and JAK kinase activity, for the prevention, treatment, treatment and reduce protein kinase, in particular JAK kinase activity mediated diseases or disorders. (by machine translation)

Enantioselective IrI-catalyzed carbocyclization of 1,6-enynes by the chiral counterion strategy

Barbazanges, Marion,Auge, Mylene,Moussa, Jamal,Amouri, Hani,Aubert, Corinne,Desmarets, Christophe,Fensterbank, Louis,Gandon, Vincent,Malacria, Max,Ollivier, Cyril

experimental part, p. 13789 - 13794 (2012/01/06)

Enantioenriched bicyclo[4.1.0]hept-2-enes were synthesized by Ir I-catalyzed carbocyclization of 1,6-enynes. No chiral ligands were used, CO and PPh3 were the only ligands bound to iridium. Instead, the stereochemical information was

Antiproliferative Properties of Polyamine Analogues: A Structure-Activity Study

Bergeron, Raymond J.,McManis, James S.,Liu, Charles Z.,Feng, Yang,Weimar, William R.,et al.

, p. 3464 - 3476 (2007/10/02)

A basis set of polyamine analogues was designed and synthesized.These compounds were used to initiate a systematic investigation of the role of chain length, terminal nitrogen alkyl group size, and symmetry of the methylene backbone in the antineoplastic

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