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(1S,5R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-oxabicyclo[3.1.0]hexan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

917483-13-7

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917483-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917483-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,4,8 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 917483-13:
(8*9)+(7*1)+(6*7)+(5*4)+(4*8)+(3*3)+(2*1)+(1*3)=187
187 % 10 = 7
So 917483-13-7 is a valid CAS Registry Number.

917483-13-7Relevant articles and documents

Synthesis of enantiomerically pure d- and l-bicyclo[3.1.0]hexenyl carbanucleosides and their antiviral evaluation

Park, Ah-Young,Kim, Won Hee,Kang, Jin-Ah,Lee, Hye Jin,Lee, Chong-Kyo,Moon, Hyung Ryong

, p. 3945 - 3955 (2011)

Based upon the fact that l-nucleosides have been generally known to be less cytotoxic than d-counterparts, l-bicyclo[3.1.0]hexenyl carbanucleoside derivatives with a fixed north conformation were designed and synthesized by employing a novel synthetic str

Asymmetric synthesis and biological activity of l-bicyclocarba-d4T

Moon, Hyung Ryong,Park, Ah-Young,Kim, Kyung Ran,Chun, Moon Woo,Jeong, Lak Shin

, p. 1653 - 1657 (2008/09/18)

Novel l-bicyclocarba-d4T (1), an enantiomer of d-N-MCd4T has been enantiopurely synthesized as a potent anti-HIV agent starting from (R)-epichlorohydrin using tandem alkylation, chemoselective reduction of ester in the presence of lactone functional group

Asymmetric synthesis of novel pseudo-D-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent

Park, Ah-Young,Moon, Hyung Ryong,Kim, Kyung Ran,Chun, Moon Woo,Jeong, Lak Shin

, p. 1001 - 1004 (2008/03/28)

Pseudo-d-vinylcyclopropyl nucleosides 10-12 bearing a quaternary carbon were designed and synthesized starting from (R)-epichlorohydrin using a tandem reaction of double alkylation and lactonization via oxirane-ring opening reaction, a Wittig reaction, an

Synthesis of novel l-N-MCd4T as a potent anti-HIV agent

Park, Ah-Young,Moon, Hyung Ryong,Kim, Kyung Ran,Chun, Moon Woo,Jeong, Lak Shin

, p. 4065 - 4067 (2008/09/19)

l-N-MCd4T (1) has been synthesized as a potent anti-HIV agent starting from (R)-epichlorohydrin using tandem alkylation, chemoselective reduction of ester in the presence of lactone functional group, RCM reaction and Mitsunobu reaction as key steps and wa

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