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(1R,6S,7R,8S)-N-benzyl-7-<(benzyloxy)methyl>bicyclo<4.3.0>non-3-en-8-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158267-48-2

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158267-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158267-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,2,6 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 158267-48:
(8*1)+(7*5)+(6*8)+(5*2)+(4*6)+(3*7)+(2*4)+(1*8)=162
162 % 10 = 2
So 158267-48-2 is a valid CAS Registry Number.

158267-48-2Relevant academic research and scientific papers

Methods of treating disease through the administration of a manzamine analog or derivative

-

, (2008/06/13)

A method of treating cancer, inflammatory disease or an infectious disease or condition in a subject in need of such treatment is disclosed. The method comprises administering to a subject an effective amount of a manzamine, or a rationally modified manzamine derivative or analog or an optical isomer or racemate or tautomer thereof or a pharmaceutically acceptable salt or prodrug thereof generated through optimized fermentation of a Micromonospora sp., extraction from sponges and then modified through semisynthesis.

Total synthesis of (+)-papuamine: An antifungal pentacyclic alkaloid from a marine sponge, Haliclona sp.

Barrett,Boys,Boehm

, p. 685 - 699 (2007/10/03)

The total synthesis of (+)-papuamine, the antipode of the C2-symmetric, optically active, pentacyclic diamine natural product, starting from a chiral diol is described. The diol is available via an asymmetric Diels-Alder reaction between 1,3-bu

Total Synthesis of (+)-Papuamine: Determination of the Absolute Stereochemistry of the Natural Product

Barrett, Anthony G. M.,Boys, Mark L.,Boehm, Terri L.

, p. 1881 - 1882 (2007/10/02)

The total synthesis of (+)-papuamine has been completed using an intramolecular Pd0 catalysed (Stille) coupling reaction to close the central diazadiene macrocycle unit.

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