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2,7-Diazaspiro[4.5]decane-1,10-dione, 3-(2-hydroxyethyl)-2-(phenylmethyl)-7-(phenylsulfonyl)-, (3S,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

566905-10-0

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566905-10-0 Usage

General Description

2,7-Diazaspiro[4.5]decane-1,10-dione, 3-(2-hydroxyethyl)-2-(phenylmethyl)-7-(phenylsulfonyl)-, (3S,5R)- is a chemical compound that belongs to the class of diazaspiro compounds. It has a molecular formula of C21H23NO5S and a molecular weight of 397.48 g/mol. 2,7-Diazaspiro[4.5]decane-1,10-dione, 3-(2-hydroxyethyl)-2-(phenylmethyl)-7-(phenylsulfonyl)-, (3S,5R)- has potential pharmaceutical applications and may exhibit biological activity. Its specific stereochemistry, with a 3S,5R configuration, and the presence of a hydroxyethyl group, phenylmethyl group, and phenylsulfonyl group, contribute to its potential pharmacological properties. Further research is needed to fully understand the potential uses of 2,7-Diazaspiro[4.5]decane-1,10-dione, 3-(2-hydroxyethyl)-2-(phenylmethyl)-7-(phenylsulfonyl)-, (3S,5R)- in the field of medicine or other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 566905-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,9,0 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 566905-10:
(8*5)+(7*6)+(6*6)+(5*9)+(4*0)+(3*5)+(2*1)+(1*0)=180
180 % 10 = 0
So 566905-10-0 is a valid CAS Registry Number.

566905-10-0Upstream product

566905-10-0Downstream Products

566905-10-0Relevant academic research and scientific papers

The first total synthesis of nakadomarin A

Nagata, Toshiaki,Nakagawa, Masako,Nishida, Atsushi

, p. 7484 - 7485 (2007/10/03)

(-)-Nakadomarin A is a member of manzamine alkaloid isolated from a marine sponge and have a unique hexacyclic structure. The first total synthesis of (+)-nakadomarin A, an enantiomer of natural product, has been accomplished from stereochemically defined 4-oxopiperidin-3-carboxylic acid derivative. The synthesis established the structure of nakadomarin A including absolute configuration. Copyright

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