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(3aR,6aS)-6a-Allyl-1-((R)-2-hydroxy-1-phenyl-ethyl)-hexahydro-cyclopenta[b]pyrrol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

250595-63-2

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250595-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250595-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,5,9 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 250595-63:
(8*2)+(7*5)+(6*0)+(5*5)+(4*9)+(3*5)+(2*6)+(1*3)=142
142 % 10 = 2
So 250595-63-2 is a valid CAS Registry Number.

250595-63-2Downstream Products

250595-63-2Relevant academic research and scientific papers

Concise stereoselective routes to advanced intermediates related to natural and unnatural pinnaic acid

Carson,Kim,Hentemann,Trauner,Danishefsky

, p. 4450 - 4452 (2007/10/03)

Important intermediates: In an effort to synthesize and determine the stereo-chemistry of pinnaic acid, C14-epimeric aldehydes 1 and 2 were generated from Meyers' lactam 3. A key step in the parallel syntheses is a highly stereoselective vinylogous Michae

Total synthesis of (+)-halichlorine: An inhibitor of VCAM-1 expression

Trauner, Dirk,Schwarz, Jacob B.,Danishefsky, Samuel J.

, p. 3542 - 3545 (2007/10/03)

The diastereoselective addition of the highly functionalized organozinc compound 1 to the aldehyde 2 in the presence of the chiral amino alcohol 3 (a??4) is a key step in the first total synthesis of (+)-halichlorine. A series of protections/deprotections

Studies towards the total synthesis of halichlorine: Asymmetric synthesis of the spiroquinolizidine subunit

Trauner, Dirk,Danishefsky, Samuel J.

, p. 6513 - 6516 (2007/10/03)

The C1-C15 spiroquinolizidine subunit (cf. 2) of the marine natural product halichlorine (1) was prepared in 12 steps starting from the known 'Meyers-lactam' 5. The synthesis involves a B-alkyl-Suzuki coupling followed by a highly stereoselective intramolecular Michael addition and an intramolecular Mannich ring closure.

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