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methyl 3,4-dideoxy-4-c-methyl-6-o-trityl-α-D-glycero-hex-3-enopyranosid-2-ulose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79607-37-7

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79607-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79607-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79607-37:
(7*7)+(6*9)+(5*6)+(4*0)+(3*7)+(2*3)+(1*7)=167
167 % 10 = 7
So 79607-37-7 is a valid CAS Registry Number.

79607-37-7Relevant academic research and scientific papers

Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses

Kawauchi, Nobuya,Sato, Ken-ichi,Yoshimura, Juji,Hashimoto, Hironobu

, p. 1433 - 1440 (2007/10/02)

Three hexopyranosides having gem-di-C-methyl group at 2- or 4-positions were synthesized by Michael addition to 2-enopyranosid-4-ulose and 3-enopyranosid-2-ulose derivatives, respectively, followed by hydroboration.A heptopyranosid-6-ulose having gem-di-C-methyl group at C-4 was also synthesized from 4-enopyranosid-6-ulose derivative in a similar way.

TWO COMPLEMENTARY METHODS FOR INTRODUCTION OF gem-DIMETHYL GROUP IN HEXOPYRANOSIDE RING

Hashimoto, Hironobu,Kawauchi, Nobuya,Yoshimura, Juji

, p. 965 - 968 (2007/10/02)

Hexopyranosides having a gem-dimethyl group in the pyranose ring were synthesized by reductive cleavage of spiro-cyclopropane derivatives and by addition of methyl cuprates to methyl-branched enolone derivatives.

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