18366-59-1 Usage
Chemical structure
A thieno[3,2-b]pyridin-6-yl ring attached to a ketone functional group through an ethanone linker.
Class of compounds
Ketones, characterized by the presence of a carbonyl group (C=O) bonded to two carbon atoms.
Heterocyclic ring system
The thieno[3,2-b]pyridin-6-yl group contains both sulfur and nitrogen atoms.
Pharmaceutical and agrochemical applications
Commonly found in compounds used in the pharmaceutical and agrochemical industries.
Organic synthesis
The presence of both the thieno[3,2-b]pyridin-6-yl and ketone functional groups gives 1-(thieno[3,2-b]pyridin-6-yl)ethanone potential for various applications in organic synthesis.
Medicinal chemistry
The compound may have potential applications in medicinal chemistry due to its unique chemical structure and functional groups.
Material science
The compound may also have potential applications in material science, given its unique chemical structure and properties.
Solubility
The solubility of 1-(thieno[3,2-b]pyridin-6-yl)ethanone in various solvents may vary depending on the specific solvent and conditions.
Stability
The stability of 1-(thieno[3,2-b]pyridin-6-yl)ethanone may depend on factors such as temperature, light exposure, and the presence of other reactive substances.
Reactivity
The reactivity of 1-(thieno[3,2-b]pyridin-6-yl)ethanone may depend on the specific reaction conditions and the presence of other reactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 18366-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,6 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18366-59:
(7*1)+(6*8)+(5*3)+(4*6)+(3*6)+(2*5)+(1*9)=131
131 % 10 = 1
So 18366-59-1 is a valid CAS Registry Number.
18366-59-1Relevant articles and documents
α-vinylation of β-aminothiophene derivatives. Synthesis of 6- functionalized thieno[3,2-b]pyridines
Berkaoui, M'hamed,Outurquin, Francis,Paulmier, Claude
, p. 9055 - 9066 (2007/10/03)
The acid-catalyzed reductive α-alkylation of β-aminothiophenes was applied to the N-(thien-3-yl)acetamide and alkyl N-(thien-3-yl)carbamates. Without reduction, β-amino α-vinylthiophenes were obtained when α-branched aldehydes were used. β-(3-Aminothien-2-yl)α,β-unsaturated ketones, esters and nitriles were also prepared from the corresponding α-functionalized acetals. These amines are intermediates in the formation of thieno[3,2- b]pyridines bearing a functional group at the β-position of the pyridine ring.
BIOMIMETIC REDUCTION WITH NON WATER-SENSITIVE NADH MODELS
Cazin, J.,Dupas, G.,Bourguignon, J.,Queguiner, G.
, p. 2375 - 2378 (2007/10/02)
Two NADH models were synthesized which are considerably less water-sensitive than classical-1,4 dihydronicotinamide derivatives such as N-benzyl-1,4 dihydronicotinamide (BNAH): these two models are reactive and more stable in the presence of water than previously reported models.
