945632-52-0 Usage
General Description
1,3-Propanediol, 2-amino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl) is a chemical compound with the molecular formula C23H41NO2. It is a derivative of 1,3-propanediol, a colorless, odorless, and slightly viscous liquid commonly used in the production of polymers and cosmetics. The addition of the 2-amino-2-(1,2,3,4-tetrahydro-6-octyl-2-naphthalenyl) group to the 1,3-propanediol molecule introduces an aromatic ring and an amine functional group, which may confer additional properties to the compound. This chemical may have potential applications in the fields of pharmaceuticals, organic synthesis, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 945632-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 945632-52:
(8*9)+(7*4)+(6*5)+(5*6)+(4*3)+(3*2)+(2*5)+(1*2)=190
190 % 10 = 0
So 945632-52-0 is a valid CAS Registry Number.
945632-52-0Relevant articles and documents
Stereochemistry-activity relationship of orally active tetralin S1P agonist prodrugs
Ma, Bin,Guckian, Kevin M.,Lin, Edward Yin-Shiang,Lee, Wen-Cherng,Scott, Daniel,Kumaravel, Gnanasambandam,Macdonald, Timothy L.,Lynch, Kevin R.,Black, Cheryl,Chollate, Sowmya,Hahm, Kyungmin,Hetu, Gregg,Jin, Ping,Luo, Yi,Rohde, Ellen,Rossomando, Anthony,Scannevin, Robert,Wang, Joy,Yang, Chunhua
scheme or table, p. 2264 - 2269 (2010/07/05)
Modifying FTY720, an immunosuppressant modulator, led to a new series of well phosphorylated tetralin analogs as potent S1P1 receptor agonists. The stereochemistry effect of tetralin ring was probed, and (-)-(R)-2-amino-2-((S)-6-octyl-1,2,3,4-tetrahydrona
BICYCLIC SPHINGOSINE 1-PHOSPHATE ANALOGS
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Page/Page column 33-34, (2008/06/13)
Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.
