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(1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.02,6]undecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74808-16-5

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74808-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74808-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,0 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74808-16:
(7*7)+(6*4)+(5*8)+(4*0)+(3*8)+(2*1)+(1*6)=145
145 % 10 = 5
So 74808-16-5 is a valid CAS Registry Number.

74808-16-5Downstream Products

74808-16-5Relevant academic research and scientific papers

An extremely mild and general method for the stereocontrolled construction of 1,2-cis-glycosidic linkages via S-glycopyranosyl phosphorodiamidimidothioates

Hashimoto, Shun-Ichi,Honda, Takeshi,Ikegami, Shiro

, p. 4769 - 4772 (2007/10/02)

A highly stereocontrolled construction of 1,2-cis-glycosidic linkages under extremely mild reaction conditions has been developed by using S-glycopyranosyl N,N,N′,N′-tetramethyl-N-phenylphosphorodiamidimidothioates with a non-participating O-2-benzyl grou

A MILD AND RAPID 1,2-TRANS-GLYCOSIDATION METHOD VIA BENZOYL-PROTECTED GLYCOPYRANOSYL P,P-DIPHENYL-N-(p-TOLUENESULFONYL)PHOSPHINIMIDATES

Hashimoto, Shun-ichi,Honda, Takeshi,Ikegami, Shiro

, p. 775 - 778 (2007/10/02)

A highly efficient 1,2-trans-glycosidation reaction with a range of acid-labile alcohols has been developed by employing benzoyl-protected glycopyranosyl P,P-diphenyl-N-(p-toluenesulfonyl)phosphinimidates as glycosyl donors.

A Rapid and Efficient Synthesis of 1,2-trans-β-Linked Glycosides via Benzyl- or Benzoyl-protected Glycopyranosyl Phosphates

Hashimoto, Shun-ichi,Honda, Takeshi,Ikegami, Shiro

, p. 685 - 687 (2007/10/02)

A highly stereocontrolled construction of 1,2-trans-β-glycosidic linkage with or without neighbouring-group participation has been achieved using benzyl- or benzoyl-protected glycopyranosyl phosphates as glycosyl donors in the presence of trimethylsilyl t

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