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4-[(1S,2R,3R,4R,5R)-1-(tert-butyldimethylsilanyloxy)-4-hydroxy-5-(4-methoxy-phenoxy)-3-methyl-2-triethylsilanyloxy-hept-6-enyl]4-methyl-[1,3]-dioxolan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

228419-61-2

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228419-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228419-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,4,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 228419-61:
(8*2)+(7*2)+(6*8)+(5*4)+(4*1)+(3*9)+(2*6)+(1*1)=142
142 % 10 = 2
So 228419-61-2 is a valid CAS Registry Number.

228419-61-2Downstream Products

228419-61-2Relevant academic research and scientific papers

Synthesis of the C(29)-C(45) bis-pyran subunit (E-F) of spongistatin 1 (altohyrtin A)

Micalizio,Pinchuk,Roush

, p. 8730 - 8736 (2007/10/03)

A synthesis of the C(29)-C(45) bis-pyran subunit 2 of spongistatin 1 (1a) is described. The synthesis proceeds in 19 steps from the chiral aldehyde ent-7, and features highly diastereoselective α-alkoxyallylation reactions using the γ-alkoxy substituted allylstannanes 17 and 19, as well as a thermodynamically controlled intramolecular Michael addition to close the F-ring pyran. The E ring was assembled via the Mukaiyama aldol reaction of F-ring methyl ketone 3 and the 2,3-syn aldehyde 4.

Towards the synthesis of spongistatin 1: Diastereoselective synthesis of the C(36)-C(45) subunit

Micalizio, Glenn C.,Roush, William R.

, p. 3351 - 3354 (2007/10/03)

An efficient and highly diastereoselective 12 step synthesis of the C(36)-C(45) subunit (2a) of spongistatin 1 is described. The synthesis features highly diastereoselective α-alkoxyallylation reactions using the γ-alkoxy substituted allylstannanes 5 and

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