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(4R,5S)-4-benzyl-3-[(tert-butoxy)carbonyl]-2,2-dimethyl-1,3-oxazolidine-5-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139397-07-2

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139397-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139397-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,9 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 139397-07:
(8*1)+(7*3)+(6*9)+(5*3)+(4*9)+(3*7)+(2*0)+(1*7)=162
162 % 10 = 2
So 139397-07-2 is a valid CAS Registry Number.

139397-07-2Relevant academic research and scientific papers

A practical diastereoselective synthesis of (?)-bestatin

Shang, Suisheng,Willems, Andreas V.,Chauhan, Satendra S.

, (2018/02/16)

Diastereoselective addition of nitromethane to Boc-D-Phe-H in the presence of sodium hydride in diethyl ether/hexane containing 15-crown-5 and subsequent N,O-protection with 2,2-dimethoxypropane gave trans-oxazolidine in a diastereomeric ratio of >16:1. T

Asymmetric reaction of simple nitro compounds with chiral 1,3-oxazolidin-2-ones

Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz

, p. 1724 - 1736 (2007/10/03)

The chiral oxazolidinone 1 (=[(3aS,6R,7aR)-tetrahydro-8,8-dimethyl-2-oxo4H- 3a,6-methano-1,3-benzoxazol-3-yl](oxo)acetaldehyde) was found to react stereoselectively with simple nitro compounds in the presence of Al 2O3 or Bu4/s

Asymmetric Nitroaldol Reaction. Synthesis of Taxotere Side Chain and (-)-Bestatin Using (1R)-8-Phenylmenthyl Glyoxylate

Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz

, p. 2844 - 2850 (2007/10/03)

The nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate (3b) with 1-nitro-1-phenylmethane (4) or with 1-nitro-2-phenylethane (13) led stereoselectively to adducts syn-2b and syn-12b, which were then transformed into the Taxotere side chain and (-)-best

Synthesis of (-)-bestatin and the Taxotere side-chain via nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate

Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz

, p. 8685 - 8687 (2007/10/03)

The nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate 6 with 1-nitro-2-phenylethane or with phenylnitromethane led stereoselectively to adducts 4 and 12, which where then transformed into (-)-bestatin hydrochloride and the Taxotere side-chain in over

Development of selective tight-binding inhibitors of leukotriene A4 hydrolase

Yuan,Munoz,Wong,Haeggstrom,Wetterholm,Samuelsson

, p. 211 - 220 (2007/10/02)

Leukotriene A4 hydrolase is a zinc-containing enzyme which exhibits both epoxide hydrolase and aminopeptidase activities. Since the enzyme product leukotriene B4 is an inflammatory mediator, it is of interest to develop selective inh

Tuftsin derivatives

-

, (2008/06/13)

Linear or cyclic tetra peptide derivatives of tuftsin which activate immunocompetent cells, i.e., macrophages and polymorphonuclear leukocyte, provide a host-mediated inhibition of the growth of tumors, provide protective effects for infectious diseases s

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