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(1R,2R)-(-)-2-bromo-1-acetoxyindan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85354-34-3

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85354-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85354-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85354-34:
(7*8)+(6*5)+(5*3)+(4*5)+(3*4)+(2*3)+(1*4)=143
143 % 10 = 3
So 85354-34-3 is a valid CAS Registry Number.

85354-34-3Relevant academic research and scientific papers

The absolute configuration of 2-bromo-2,3-dihydro-1H-inden-1-ols

Prysiazhnuk, Dmitry V.,Rusanov, Eduard B.,Kolodiazhnyi, Oleg I.

supporting information, p. 3023 - 3031 (2021/08/13)

All four possible stereoisomers of cis- and trans-2-bromo-2,3-dihydro-1H-inden-1-ols, which are important intermediates in the synthesis of biologically active compounds, were synthesized and their configurations were studied by enzymatic kinetic resoluti

A useful propionate cofactor enhancing activity for organic solvent-tolerant recombinant metal-free bromoperoxidase (perhydrolase) from Streptomyces aureofaciens

China, Hideyasu,Ogino, Hiroyasu

, p. 327 - 332 (2019/07/12)

The oxidative brominating activity of an organic solvent-tolerant recombinant metal-free bromoperoxidase BPO-A1 with C-terminal His-tag (rBPO-A1), from Streptomyces aureofaciens found to depend on various additives. These included carboxylic acids, used as cofactors and alcohols, used as water-miscible organic solvents. Enzyme activity was significantly enhanced by using propanoic acid (PA) as a cofactor, which had a high Log D at pH 5.0 and ethylene glycol with a low Log P. The positional specificity of oxidative hydroxybromination for olefins, using rBPO-A1 and PA in the presence of methanol, was higher compared to a non-enzymatic reaction using peracetic acid. The oxidative bromination step, occurring after enzymatic peroxidation step, is suggested to be pseudoenzymatic.

Lipase-mediated resolution of indene bromohydrin

Igarashi, Yoshio,Otsutomo, Shinya,Harada, Masayuki,Nakano, Shigeru,Watanabe, Shoji

, p. 549 - 552 (2007/10/03)

Lipase-mediated resolution of indene bromohydrin was examined, and we have found that immobilized CAL (Candida antarctica lipase SP525 immobilized on acurrell) was an efficient biocatalyst to resolve a readily available racemic indene bromohydrin (+)-1. Enantiomerically enriched (1R,2R)-2- bromoindan-1-ol (-)-1 and its (1S,2S)-acetate (+)-2 were obtained by this method.

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