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(E)-(2R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-5-{2-[(2S,3R)-2-(4-methoxy-benzyloxy)-4-((1S,3R,4R)-3-methoxy-4-triisopropylsilanyloxy-cyclohexyl)-3-methyl-butyl]-[1,3]dithian-2-yl}-3-methyl-hex-3-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

164714-15-2

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164714-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164714-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,1 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 164714-15:
(8*1)+(7*6)+(6*4)+(5*7)+(4*1)+(3*4)+(2*1)+(1*5)=132
132 % 10 = 2
So 164714-15-2 is a valid CAS Registry Number.

164714-15-2Upstream product

164714-15-2Relevant academic research and scientific papers

A unified total synthesis of the immunomodulators (-)-rapamycin and (-)-27-demethoxyrapamycin: Construction of the C(21-42) perimeters

Smith III, Amos B.,Condon, Stephen M.,McCauley, John A.,Leazer Jr., Johnnie L.,Leahy, James W.,Maleczka Jr., Robert E.

, p. 947 - 961 (2007/10/03)

A total synthesis of the potent, naturally occurring immunomodulators (-)-rapamycin (1) and (-)-27-demethoxyrapamycin (2) has been achieved via a unified, highly convergent synthetic strategy. Both targets were elaborated from common building blocks A-E,

Rapamycin synthetic studies. 1. Construction of the C(27)-C(42) subunit

Smith III, Amos B.,Condon, Stephen M.,McCauley, John A.,Leahy, James W.,Leazer Jr., Johnnie L.,Maleczka Jr., Robert E.

, p. 4907 - 4910 (2007/10/02)

A convergent synthetic approach to the C(27)-C(42) fragment of the immunosuppressive macrocycle rapamycin is described.

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