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108741-14-6

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108741-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108741-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108741-14:
(8*1)+(7*0)+(6*8)+(5*7)+(4*4)+(3*1)+(2*1)+(1*4)=116
116 % 10 = 6
So 108741-14-6 is a valid CAS Registry Number.

108741-14-6Relevant articles and documents

Catalysts/cosolvents and general acid catalysts for acceleration of the hydrolysis of osmate(VI) esters

Junttila, Mikko H.,Hormi, Osmo E.O.

, p. 3430 - 3432 (2010)

New catalysts/cosolvents as hydrolysis aids and the properties of the catalyst/cosolvent that effect the efficiency of the hydrolysis aid for the hydrolysis of osmate(VI) esters of aliphatic olefins are presented. Also, the effect of pH of the reaction media on the specific and general acid-catalysed hydrolysis of osmate(VI) esters of conjugated aromatic olefins is presented.

RAS INHIBITORS

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Paragraph 1294-1295, (2021/05/07)

The disclosure features macrocyclic compounds, and pharmaceutical compositions and protein complexes thereof, capable of inhibiting Ras proteins, and their uses in the treatment of cancers.

Investigation for the cyclization efficiency of linear tetrapeptides: Synthesis of tentoxin B and dihydrotentoxin

Sato, Ryota,Oyama, Kie,Konno, Hiroyuki

supporting information, p. 6173 - 6181 (2018/09/17)

Investigation of the cyclization efficiency of N-methyl linear tetrapeptides using a molecular modeling study and chemical synthesis is described. The linear peptide with two N-methyl groups, MeAla-Leu-MePhe-Gly, forms γ-turn like conformation with the am

Highly enantioselective synthesis of anti aryl β-hydroxy α-amino esters via DKR transfer hydrogenation

Liu, Zhuqing,Shultz, C.Scott,Sherwood, Candice A.,Krska, Shane,Dormer, Peter G.,Desmond, Richard,Lee, Claire,Sherer, Edward C.,Shpungin, Joseph,Cuff, James,Xu, Feng

scheme or table, p. 1685 - 1688 (2011/05/05)

An efficient preparation of highly enantiomerically enriched aryl β-hydroxy α-amino esters via dynamic kinetic resolution (DKR), asymmetric transfer hydrogenation of α-amino β-keto esters is described. The anti β-hydroxyl α-amino esters were obtained both in high yields and high diasteroselectivity. The observed high anti selectivity is inconsistent with the previous results in literature. The absolute stereochemistry of the aryl β-hydroxy α-amino esters was unambiguously confirmed via chemical derivatization as well as Vibrational Circular Dichroism (VCD) techniques.

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