195311-91-2 Usage
Molecular structure
The compound consists of a butanol molecule attached to an amino group, along with two 3,4-dimethoxyphenyl groups.
Classification
It is a secondary amine.
Chirality
The compound is chiral, with two enantiomers.
Configuration
The (2S)configuration is specifically mentioned in the name of the compound.
Properties
The exact uses and properties of this specific compound would likely depend on its enantiomeric form and the specific nature of the chemical reactions in which it is involved.
Check Digit Verification of cas no
The CAS Registry Mumber 195311-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 195311-91:
(8*1)+(7*9)+(6*5)+(5*3)+(4*1)+(3*1)+(2*9)+(1*1)=142
142 % 10 = 2
So 195311-91-2 is a valid CAS Registry Number.
195311-91-2Relevant academic research and scientific papers
A simple and efficient synthetic route to chiral isopavines. Synthesis of (-)-O-methylthalisopavine and (-)-amurensinine
Carrillo, Luisa,Badia, Dolores,Dominguez, Esther,Vicario, Jose L.,Tellitu, Imanol
, p. 6716 - 6721 (2007/10/03)
The isopavinan alkaloids (-)-O-methylthalisopavine (7a) and (-)- amurensinine (7d) have been synthesized in good yield and high ee from the appropriate 1,2-diarylethylamine derivatives using optically active β-amino alcohols as chiral support. This synthetic route employs as key steps the alkylation reaction of the azomethine derivatives 2 with Grignard reagents 1 and-a novel one-pot double-intramolecular cyclization of the adequately functionalized 1,2-diarylethylamines 5 to afford a series of optically active isopavines 6a-d and 7a-d.
