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(2R,3R)-1,2-Dichloro-3,4-dimethoxy-butane is a chiral organic compound with the molecular formula C6H12Cl2O2. It features a butane backbone with two chlorine atoms at the 1st and 2nd carbon positions, and two methoxy groups at the 3rd and 4th carbon positions. The compound exhibits stereochemistry, with the R configuration at both the 2nd and 3rd carbon atoms. This specific arrangement of substituents endows the molecule with unique chemical and physical properties, making it potentially useful in various applications, such as in the synthesis of pharmaceuticals or as a chiral building block in organic chemistry.

76465-35-5

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76465-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76465-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76465-35:
(7*7)+(6*6)+(5*4)+(4*6)+(3*5)+(2*3)+(1*5)=155
155 % 10 = 5
So 76465-35-5 is a valid CAS Registry Number.

76465-35-5Downstream Products

76465-35-5Relevant academic research and scientific papers

Three-Component Reactions. IX. Methoxychlorination of Butadiene. 1. Composition of Reaction Mixtures Obtained Using Either an Excess of Butadiene or an Excess of Chlorine

Beger, J.,Schiefer, H.,Movsumzade, M.M.,Gurbanov, P.A.

, p. 599 - 609 (2007/10/02)

Methoxychlorination of butadiene with 2 mol chlorine gives saturated secondary addition products 5-15, which were found identical with methoxychlorination products of unsaturated primary addition products 1-4 (investigated by capillar GLC). 1,2 and 3 add chlorine and methanol with high regioselectivity (80-90percent); meso and erythro isomer predominate in MARKOVNIKOV products from 1 and 2 (87percent diastereoselectivity). 5-7 and 11-15 were separated by preparative GLC for structural analysis.

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