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(2R)-3-benzyloxy-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-2H-furan-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86404-08-2

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86404-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86404-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86404-08:
(7*8)+(6*6)+(5*4)+(4*0)+(3*4)+(2*0)+(1*8)=132
132 % 10 = 2
So 86404-08-2 is a valid CAS Registry Number.

86404-08-2Relevant articles and documents

ASCORBIC ACID-RELATED COMPOUND AND ANTI-PLANT-VIRUS AGENT

-

, (2015/09/22)

The present invention provides a compound represented by formula (1) (wherein each of X1 and X2 independently represents -OR1, -NR2R3 or -CR4R5R6 or the like, each of

3-O and 2-C Alkylation of L-ascorbates with benzyl halides and N-substituted indolemethanol derivatives

Korolev,Luzikov,Reznikova,Preobrazhenskaya

experimental part, p. 457 - 462 (2011/02/17)

Coupling of alkali metal ascorbates with benzyl halides and 2and 3-hydroxymethylindole methanesulfonates resulted in L-ascorbic acid 3-Oand 2-C-derivatives. In contrast to 3-Obenzyl L-ascorbate, its indole analogs are unstable compounds, which underwent decomposition or rearrangement during isolation to give thermodynamically stable 2-C-isomers.

Regioselectiv O-alkylation of ascorbic acid for the of efficient synthesis if antioxidants

Beifuss, Uwe

, p. 147 - 149 (2007/10/03)

The first chemo- and regioselective alkylation of ascorbic acid without protection of the hydroxyl groups at C-5 and C-6 exclusively yields the corresponding 3-O-ethers which can be used to synthesize the 2,3-O,O-diethers as well as the 2-0-alkyl ethers o

Organoalane-mediated isomerization of ascorbic and isoascorbic acid derivatives

Schachtner, Josef,Stachel, Hans-Dietrich

, p. 3263 - 3276 (2007/10/03)

Derivatives of L-ascorbic acid 2a, 10a/11a and D-isoascorbic acid 2b, 10b/11b, when treated with triisobutylaluminium, partly epimerize to give the corresponding derivatives of L-isoascorbic acid ent-2b, ent-10b or D-ascorbic acid ent-2a, ent-10a, ent-11a, respectively. Complete removal of the protecting groups is effected by hydrogenolysis of the benzylidene acetals ent-10 and ent-11a. This reaction leads to D-ascorbic acid ent-1a or L-isoascorbic acid ent-1b, respectively. Furthermore, the four acetonides 2 were converted by ozonolysis, transesterification and finally catalytic hydrogenation to the threonic and erythronic acid ketals 9. Copyright (C) Elsevier Science Ltd.

Ascorbic acid ethers in angiogene

-

, (2008/06/13)

Ethers of ascorbic and isoascorbic acid and ketals and acetals thereof, angiogenesis inhibitors.

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