135675-29-5 Usage
Chemical class
Isoquinolines A class of organic compounds containing a benzene ring fused to a pyridine ring.
Furan ring
A five-membered ring with one double bond and four carbon atoms, fused to the tetrahydroisoquinoline ring.
Tetrahydroisoquinoline ring
A partially saturated isoquinoline ring with four hydrogen atoms added to the carbon framework.
Unique and complex molecule
The fusion of the furan and tetrahydroisoquinoline rings creates a unique and complex molecular structure.
Potential pharmacological applications
Due to its structure and biological activities, this compound may have various applications in the field of medicine.
Building block in drug synthesis
It can be used as a starting point or intermediate in the synthesis of various drugs and pharmaceutical compounds.
Biological activities
The compound may exhibit properties such as anticancer, anti-inflammatory, or analgesic effects, which could be valuable for medicinal research.
Further research needed
More research and exploration of the compound's potential uses and pharmacological properties are necessary to fully understand its utility in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 135675-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,7 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135675-29:
(8*1)+(7*3)+(6*5)+(5*6)+(4*7)+(3*5)+(2*2)+(1*9)=145
145 % 10 = 5
So 135675-29-5 is a valid CAS Registry Number.
135675-29-5Relevant articles and documents
A new approach to construction of isoindolo[1,2-a]isoquinoline alkaloids Nuevamine, Jamtine, and Hirsutine via IMDAF reaction
Zubkov, Fedor I.,Ershova, Julya D.,Orlova, Anna A.,Zaytsev, Vladimir P.,Nikitina, Eugeniya V.,Peregudov, Alexandr S.,Gurbanov, Atash V.,Borisov, Roman S.,Khrustalev, Victor N.,Maharramov, Abel M.,Varlamov, Alexey V.
, p. 3789 - 3803 (2009)
The interaction between 1-furyl-1,2,3,4-tetrahydroisoquinolines and unsaturated acids derivatives (acryloyl, methacryloyl, and crotonoyl chloride, maleic and citraconic anhydride) was studied. It was shown that the reaction proceeds via amide formation an
