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(3S,4S)-4-benzyloxy-tetrahydro-furan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183387-07-7

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183387-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183387-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,3,8 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 183387-07:
(8*1)+(7*8)+(6*3)+(5*3)+(4*8)+(3*7)+(2*0)+(1*7)=157
157 % 10 = 7
So 183387-07-7 is a valid CAS Registry Number.

183387-07-7Relevant academic research and scientific papers

Process for the preparation of trans-3-alkyloxy-4-hydroxytetrahydrofuran

-

, (2008/06/13)

Disclosed is a process for preparing novel trans-3-alkyloxy-4-hydroxytetrahydrofurans including racemic and substantially enantiomerically pure (3S,4S)-trans-3-alk(en)yloxy-4-hydroxytetrahydrofurans and (3R,4R)-trans-3-alk(en)yloxy-4-acyloxytetrahydrofura

Tetrahydrofuran Ring-Containing Nucleotide Analogs Related to HPMPA and PMEA

Liboska, Radek

, p. S72 - S75 (2007/10/03)

Synthesis of 9-N-(4-(phosphonomethoxy)tetrahydrofuran-3-yl)adenine derivatives, a novel type of nucleotide analogs related to (R)- and (S)-9-N-(3-hydroxy-2-phosphonomethoxypropyl)adenine ((R)- and (S)-HPMPA) and 9-(2-phosphonomethoxyethyl)adenine (PMEA), is described.The synthesis of adenine nucleotide analogs 6a-6d is based on the reaction of 6-N-protected adenine derivatives 5a-5d with diisopropyl tosyloxymethanephosphonate and subsequent deprotection of resulting compounds.The starting "nucleoside" derivatives have been prepared from chiral 4-benzyloxytetrahydrofuran-3-ols 3a-3d.

Enzymic Preparation of Tetrahydrofuran Derivatives of High Optical Purity

Seemayer, Robert,Schneider, Manfred P.

, p. 2359 - 2360 (2007/10/02)

3,4-Disubstituted tetrahydrofurans (1)-(4) and (7) of high optical purities have been prepared by enantioselective enzyme hydrolysis of their acetates (+/-)-(1a) - (4a) and (7a) using a lipase from Pseudomonas sp. (SAM-II).

NOVEL (4+1) FRAGMENT COMBINATION APPROACH TO CHIRAL CYCLOPENTANOIDS FROM TARTARIC ACID

Barriere, Francoise,Barriere, Jean-Claude,Barton, Derek H. R.,Cleophax, Jeanine,Gateau-Olesker, Alice,et al.

, p. 3121 - 3124 (2007/10/02)

A chiral cyclopentanoid building block 29 has been synthesized in a "one pot" cyclization process from epoxides 22-25 (which are readily accessible from (R,R)-(+)-tartaric acid) with the carbanion derived from phenylthioacetonitrile (PhS-CH2-CN).

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