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CarbaMic acid, [1-(2-broMophenyl)ethyl]-, 1,1-diMethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1086391-99-2

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1086391-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1086391-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,9 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1086391-99:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*9)+(3*1)+(2*9)+(1*9)=182
182 % 10 = 2
So 1086391-99-2 is a valid CAS Registry Number.

1086391-99-2Downstream Products

1086391-99-2Relevant academic research and scientific papers

Biocatalytic Routes to Enantiomerically Enriched Dibenz[c,e]azepines

France, Scott P.,Aleku, Godwin A.,Sharma, Mahima,Mangas-Sanchez, Juan,Howard, Roger M.,Steflik, Jeremy,Kumar, Rajesh,Adams, Ralph W.,Slabu, Iustina,Crook, Robert,Grogan, Gideon,Wallace, Timothy W.,Turner, Nicholas J.

, p. 15589 - 15593 (2017)

Biocatalytic retrosynthetic analysis of dibenz[c,e]azepines has highlighted the use of imine reductase (IRED) and ω-transaminase (ω-TA) biocatalysts to establish the key stereocentres of these molecules. Several enantiocomplementary IREDs were identified

Asymmetric Hydrogenation of Dibenzo[ c,e]azepine Derivatives with Chiral Cationic Ruthenium Diamine Catalysts

Zhang, Shanshan,Chen, Fei,He, Yan-Mei,Fan, Qing-Hua

supporting information, p. 5538 - 5541 (2019/08/01)

An efficient Ru-catalyzed asymmetric hydrogenation of dibenzo[c,e]azepines is reported. A series of seven-membered cyclic amines were obtained with moderate to excellent enantioselectivity. The catalyst counteranion played an important role in achieving high-level chiral induction. Moreover, a one-pot synthesis of chiral 6,7-dihydro-5H-dibenz[c,e]azepines via two-step reductive amination was also developed.

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

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Page/Page column 54, (2011/04/14)

A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).

TRIAZOLYL AMINOPYRIMIDINE COMPOUNDS

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Page/Page column 23, (2009/01/20)

The present invention provides triazolyl aminopyrimidine compounds useful in the treatment of cancer.

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