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2,5-anhydro-3,4-O-isopropylidene-L-arabinose N,N-dimethylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100644-82-4

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100644-82-4 Usage

Chemical composition

Composed of arabinose, isopropylidene, and hydrazone functional groups.

Derivation

Derived from L-arabinose.

Physical form

White to off-white crystalline solid.

Solubility

Soluble in organic solvents such as acetone, ethyl acetate, and chloroform.

Uses

Utilized as a reagent in the preparation of various organic compounds, used as a protecting group for the hydroxyl group in carbohydrate chemistry, and has potential applications in the pharmaceutical industry for the synthesis of novel drug compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 100644-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100644-82:
(8*1)+(7*0)+(6*0)+(5*6)+(4*4)+(3*4)+(2*8)+(1*2)=84
84 % 10 = 4
So 100644-82-4 is a valid CAS Registry Number.

100644-82-4Downstream Products

100644-82-4Relevant academic research and scientific papers

ISOPROPYLIDENATION OF L-ARABINOSE N,N-DIMETHYLHYDRAZONE

Koos, Miroslav,Mosher, Harry S.

, p. 1994 - 1999 (2007/10/02)

Direct isopropylidenation of L-arabinose N,N-dimethylhydrazone (I) was studied.Four major products whose structures were proven were produced in varying ratios depending upon the conditions. 2,2-Dimethoxypropane and sulfuric acid at 20 deg C gave a 36percent yield of 2,3:4,5-di-O-isopropylidene-L-arabinose N,N-dimethylhydrazone (II).Attempted aldol condensations directly on this hydrazone with paraformaldehyde were unsuccesful.This hydrazone was readily hydrolyzed to the corresponding protected aldehyde VI which underwent an aldol-Cannizzaro reaction to give the branched chain pentitol VII in high yield.

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