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119817-95-7

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119817-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119817-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,1 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119817-95:
(8*1)+(7*1)+(6*9)+(5*8)+(4*1)+(3*7)+(2*9)+(1*5)=157
157 % 10 = 7
So 119817-95-7 is a valid CAS Registry Number.

119817-95-7Relevant articles and documents

Lipase catalysed synthesis of optically enriched α-haloamides

Azim, Abul,Sharma, Sunil K.,Olsen, Carl E.,Parmar, Virinder S.

, p. 1345 - 1348 (2001)

An efficient lipase catalysed synthesis of optically enriched α-halogenated amides with concomitant optical enrichment of the starting α-haloesters is described. Candida antarctica lipase (CAL) was found to be a better catalyst over porcine pancreatic lipase (PPL) and Candida cylindracea lipase (CCL). The effect of different organic solvents was also studied.

DOTMA-based amides (DOTMAMs) as a platform for the development of PARACEST MRI contrast agents

Suchy,Li,Milne,Bartha,Hudson

, p. 62647 - 62655 (2016/07/16)

A synthetic methodology leading to previously unknown DOTMA-based secondary amides (DOTMAMs) has been developed. Alkylation of cyclen with l-lactic acid-derived pseudohalides was used as a key step affording the alkyl- and aryl-decorated DOTMAMs. Amino acid-decorated DOTMAMs were obtained via peptide coupling between DOTMA and protected amino acids. Metallation of the DOTMAMs ligand with Tm3+ gave complexes exhibiting proximal amide proton based paramagnetic CEST effects at -50 ppm relative to water.

Enzymatic Aminolysis and Transamidation Reactions

Gotor, Vicente,Brieva, Rosario,Gonzalez, Carmen,Rebolledo, Francisca

, p. 9207 - 9214 (2007/10/02)

Chiral amides can be obtained from (+/-)-2-chloropropionate esters and a wide range of amines when the reaction is catalyzed by Candida cylindracea lipase.The enantioselection of the enzyme in this aminolysis reaction depends on the substrate and nucleoph

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