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N-CBz-4-exo-methylene-L-proline ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169820-06-8

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169820-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169820-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,8,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169820-06:
(8*1)+(7*6)+(6*9)+(5*8)+(4*2)+(3*0)+(2*0)+(1*6)=158
158 % 10 = 8
So 169820-06-8 is a valid CAS Registry Number.

169820-06-8Relevant articles and documents

Nazumazoles A-C, cyclic pentapeptides dimerized through a disulfide bond from the marine sponge theonella swinhoei

Fukuhara, Kazuya,Takada, Kentaro,Okada, Shigeru,Matsunaga, Shigeki

, p. 2646 - 2648 (2015)

A mixture of nazumazoles A-C (1-3) was purified from the extract of the marine sponge Theonella swinhoei. The mixture was eluted as an extraordinarily broad peak in the reversed-phase HPLC. The structures of nazumazoles were determined by interpretation o

Thrombin inhibitors from the freshwater cyanobacterium Anabaena compacta

Anas, Andrea Roxanne J.,Kisugi, Takaya,Umezawa, Taiki,Matsuda, Fuyuhiko,Okino, Tatsufumi,Campitelli, Marc R.,Quinn, Ronald J.

, p. 1546 - 1552,7 (2012/12/12)

Bioassay-guided investigation of the cyanobacterium Anabaena compacta extracts afforded spumigin J (1) and the known thrombin inhibitor spumigin A (2). The absolute configuration of 1 was analyzed by advanced Marfey's methodology. Compounds 1 and 2 inhibi

Thrombin inhibitors from the freshwater cyanobacterium Anabaena compacta

Anas, Andrea Roxanne J.,Kisugi, Takaya,Umezawa, Taiki,Matsuda, Fuyuhiko,Campitelli, Marc R.,Quinn, Ronald J.,Okino, Tatsufumi

, p. 1546 - 1552 (2013/01/15)

Bioassay-guided investigation of the cyanobacterium Anabaena compacta extracts afforded spumigin J (1) and the known thrombin inhibitor spumigin A (2). The absolute configuration of 1 was analyzed by advanced Marfey's methodology. Compounds 1 and 2 inhibi

Concise, stereoselective route to the four diastereoisomers of 4-methylproline

Murphy, Annabel C.,Mitova, Maya I.,Blunt, John W.,Munro, Murray H.G.

experimental part, p. 806 - 809 (2009/04/07)

The full stereochemical characterization of 4-methylproline, a rare amino acid found in a number of peptidic secondary metabolites, has often been hindered by long reaction sequences or low stereoselectivity in the synthesis leading to reference samples. The preparation of the four diastereoisomers of 4-methylproline by a concise and stereoselective route is presented and features a six-step route with late-stage stereodivergence, good stereoselectivity for both cis- and trans-series (75% and 88% de, respectively), and good overall yields (cumulative yields of 30-40%). Additional data on the Marfey's derivatives of the stereoisomers are also presented.

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