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14099-74-2

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14099-74-2 Usage

Chemical class

Bicyclic heterocyclic compound

Family

Pyridine family

Molecular weight

163.22 g/mol

Pharmaceutical industry use

Potential therapeutic properties for neurological and psychiatric disorders

Research potential

Effects on neurotransmitter systems in the brain

Interest to professionals

Chemists and pharmacologists due to complex structure and pharmacological applications

Structural features

Decahydro (10 hydrogen atoms), 6H-pyrido[1,2-a]quinolin-6-one (indicating the presence of a six-membered nitrogen-containing ring fused to a six-membered carbon ring)

Potential applications

Development of drugs for neurological and psychiatric disorders

Research focus

Understanding the compound's interaction with neurotransmitter systems and its potential therapeutic effects

Check Digit Verification of cas no

The CAS Registry Mumber 14099-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14099-74:
(7*1)+(6*4)+(5*0)+(4*9)+(3*9)+(2*7)+(1*4)=112
112 % 10 = 2
So 14099-74-2 is a valid CAS Registry Number.

14099-74-2Downstream Products

14099-74-2Relevant articles and documents

α-C-H Bond Functionalization of Unprotected Alicyclic Amines: Lewis-Acid-Promoted Addition of Enolates to Transient Imines

Kim, Jae Hyun,Paul, Anirudra,Ghiviriga, Ion,Seidel, Daniel

supporting information, p. 797 - 801 (2021/02/06)

Enolizable cyclic imines, obtained in situ from their corresponding lithium amides by oxidation with simple ketone oxidants, are readily alkylated with a range of enolates to provide mono- and polycyclic β-aminoketones in a single operation, including the natural product (±)-myrtine. Nitrile anions also serve as competent nucleophiles in these transformations, which are promoted by BF3 etherate. β-Aminoesters derived from ester enolates can be converted to the corresponding β-lactams.

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