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7-Oxabicyclo[4.1.0]heptan-2-ol, 4-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-, (1R,2R,4S,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

677745-84-5

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677745-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 677745-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 677745-84:
(8*6)+(7*7)+(6*7)+(5*7)+(4*4)+(3*5)+(2*8)+(1*4)=225
225 % 10 = 5
So 677745-84-5 is a valid CAS Registry Number.

677745-84-5Downstream Products

677745-84-5Relevant academic research and scientific papers

Stereoselective synthesis of a novel natural carbasugar and analogues from hydroxymethylated cycloalkenone scaffolds

Rej, Rohan,Jana, Navendu,Kar, Shantasree,Nanda, Samik

experimental part, p. 364 - 372 (2012/07/16)

Novel carbasugars from Streptomyces lincolnensis have been synthesized from an enantiomerically pure 5-hydroxymethyl-cyclohex-2-enone scaffold via a stereoselective approach. Several structural analogues of those carbasugars have also been synthesized in a stereoselective manner from hydroxymethylated cycloalkenone derivatives.

Practical syntheses of enantiopure carbasugars: Carba-β-altrose, carba-β-mannose, carba-β-idose, and carba-β-talose derivatives

Yu, Seok-Ho,Chung, Sung-Kee

, p. 581 - 584 (2007/10/03)

D and L forms of carba-β-altrose 8, carba-β-mannose 10a, carba-β-idose 12, carba-β-talose 14 derivatives were prepared from (±)-3-cyclohexene-1-carboxylic acid 1. Homochiral diol compounds D-5a and L-5a, which were prepared from 1 via enzyme resolution of

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