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Carbamic acid, (6-cyclopropyl-2,3,4,5-tetrahydro-3-pyridinyl)(phenylmethyl)-, phenylmethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132256-85-0

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132256-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132256-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132256-85:
(8*1)+(7*3)+(6*2)+(5*2)+(4*5)+(3*6)+(2*8)+(1*5)=110
110 % 10 = 0
So 132256-85-0 is a valid CAS Registry Number.

132256-85-0Relevant academic research and scientific papers

Synthesis of (-)-Slaframine and Related Indolizidines

Pearson, William H.,Bergmeier, Stephen C.,Williams, John P.

, p. 3977 - 3987 (2007/10/02)

An enantioselective synthesis of the indolizidine alkaloid (-)-slaframine 1 is reported.Reductive double cyclization of the azido epoxy tosylate 48 afforded the indolizidine 52, which was converted to (-)-slaframine in two steps.The cyclization substrate

Synthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangement

Heidt, Philip C.,Bergmeier, Stephen C.,Pearson, William H.

, p. 5441 - 5444 (2007/10/02)

Cyclic imines 6a and 6b were obtained by the intramolecular 1,3-dipolar cycloaddition of azides with methylenecyclopropanes. Acid catalyzed rearrangement produced bicyclic (-)-enamines 7, which upon reduction provided indoilizidenes 8. A similar strategy was used for the synthesis of (-)-8a-epi-desacctoxyslaframine 16.

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