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(S)-5-phenylmethoxypentane-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81132-13-0

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81132-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81132-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81132-13:
(7*8)+(6*1)+(5*1)+(4*3)+(3*2)+(2*1)+(1*3)=90
90 % 10 = 0
So 81132-13-0 is a valid CAS Registry Number.

81132-13-0Downstream Products

81132-13-0Relevant articles and documents

Remote asymmetric induction in an intramolecular ionic Diels-Alder reaction: Application to the total synthesis of (+)-dihydrocompactin

Sammakia, Tarek,Johns, Deidre M.,Kim, Ganghyeok,Berliner, Martin A.

, p. 6504 - 6505 (2007/10/03)

The total synthesis of (+)-dihydrocompactin via an intramolecular ionic Diels-Alder reaction that proceeds with remote stereocontrol is described. This reaction proceeds by an intermediate vinyl-oxocarbenium ion (6), the conformational constraints of whic

Enantioselective construction of the C1-C16 segment of lasonolide A

Deba, Tatsuya,Yakushiji, Fumika,Shindo, Mitsuru,Shishido, Kozo

, p. 1500 - 1502 (2007/10/03)

An efficient and enantiocontrolled synthesis of the C1-C 16 segment of lasonolide A has been accomplished starting from a readily available optically pure aldehyde.

Pigments of fungi. XLIV* synthesis of differentially protected chiral pentane-1,3,5-triol derivatives; confirmation of the absolute configuration of naturally occurring 3-acetoxy-2,3-dihydropiptoporic acid

Burns, Christopher J.,Gill, Melvyn,Saubern, Simon

, p. 1067 - 1079 (2007/10/03)

(R)-1-t-Butyldimethylsilyloxy-5-phenylmethoxypentan-3-ol (25), prepared in 68% yield and >99.9% enantiomeric excess over six steps from commercially available but-3-yn-1-ol by Katsuki-Sharpless epoxidation, was converted by way of its 3-methoxymethyl ethe

Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 2. Simple Deoxyalditols

Ma, P.,Martin, V. S.,Masamune, S.,Sharpless, K. B.,Viti, S. M.

, p. 1378 - 1380 (2007/10/02)

Asymmetric epoxidation of allylic alcohols followed by selective hydride reduction provides a new route to chiral 1,3-diols and 1,3,5-triols; one of the 1,3,5-triols (21) is also synthesized from D-glucose.

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