43052-77-3 Usage
Description
(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile is a complex chemical compound derived from isoquinoline, a nitrogen-containing heterocyclic compound. It features a nitrile functional group and two methoxy (CH3O) functional groups, which contribute to its solubility and chemical reactivity. This unique structure and potential reactivity make it a promising candidate for various applications in pharmaceutical and chemical research.
Uses
Used in Pharmaceutical Research:
(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile is used as a building block for the synthesis of various pharmaceutical compounds due to its versatile molecular structure and potential reactivity. Its ability to interact with different functional groups makes it a valuable component in the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile serves as a key intermediate for the synthesis of a wide range of organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable tool for exploring new chemical reactions and developing novel materials.
Used in Drug Delivery Systems:
(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile can be employed as a component in the design of drug delivery systems, potentially enhancing the solubility, stability, and bioavailability of therapeutic agents. Its structural features may allow for the development of targeted drug delivery platforms, improving the efficacy and safety of various treatments.
Used in the Synthesis of Bioactive Molecules:
Due to its unique structure, (6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)acetonitrile may be utilized in the synthesis of bioactive molecules with potential applications in medicine. Its ability to form various chemical bonds and interact with different functional groups can lead to the creation of new compounds with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 43052-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,5 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 43052-77:
(7*4)+(6*3)+(5*0)+(4*5)+(3*2)+(2*7)+(1*7)=93
93 % 10 = 3
So 43052-77-3 is a valid CAS Registry Number.
43052-77-3Relevant articles and documents
6,7-Dimethoxy-3,4-dihydroisoquinolin-1(2H)-ylidenoacetonitrile in some fusion reactions
Afon'kin,Kostrikin,Shumeiko,Popov
experimental part, p. 731 - 745 (2011/08/22)
6,7-Dimethoxy-3,4-dihydroisoquinolin-1-ylacetonitrile in the enamine form readily reacts with acyl iso(thio)cyanates affording in high yields 1,2-fused oxo- and thioxodihydropyrimidoisoquinolines and thiouracyloisoquinolines. The reaction of the enamine with primary amines of diverse classes in the presence of 2 equiv of formaldehyde resulted in 1,2-fused N-substituted tetrahydropyrimidinoisoquinolines whose yields depended on the basicity and sterical accessibility of the reagent. Fused 5-hydroxyindolo-, dioxopyrrolo-, pyrroloisoquinolines formed in medium yields in the one-stage reactions of the enamine with p-benzoquinone, oxalyl chloride, and β-nitrostyrene respectively. The reaction of 1-cyanomethyl-6,7-dimethoxydihydroisoquinoline with acrylonitrile leads to the formation of 1,2-fused iminopyridinoisoquinoline easily hydrolysable to pyridine derivative and readily reacting by the amidine group with aroyl chlorides and arylsulfonyl chlorides. Pleiades Publishing, Ltd., 2011.
