33301-42-7 Usage
Uses
Used in Pharmaceutical Industry:
5,10-dimethylbenzo[g]isoquinoline is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and potential biological activities. Its presence in the development of new drugs can contribute to the discovery of novel therapeutic agents.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 5,10-dimethylbenzo[g]isoquinoline is employed as a key component in the synthesis of a range of organic compounds. Its chemical properties make it a valuable precursor for creating complex organic molecules with diverse applications.
Used in Anti-inflammatory Applications:
5,10-dimethylbenzo[g]isoquinoline is used as an anti-inflammatory agent due to its potential biological activities. Its capacity to modulate inflammatory responses may contribute to the development of treatments for various inflammatory conditions.
Used in Anticancer Research:
5,10-dimethylbenzo[g]isoquinoline is also utilized in anticancer research, where it is investigated for its potential to inhibit cancer cell growth and proliferation. Its presence in the development of new cancer therapies could lead to more effective treatments for various types of cancer.
Ongoing research is being conducted to further explore the potential uses and effects of 5,10-dimethylbenzo[g]isoquinoline, with the aim of expanding its applications across different industries and improving its therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 33301-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,0 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33301-42:
(7*3)+(6*3)+(5*3)+(4*0)+(3*1)+(2*4)+(1*2)=67
67 % 10 = 7
So 33301-42-7 is a valid CAS Registry Number.
33301-42-7Relevant academic research and scientific papers
Krapcho,Gilmor
, p. 669 - 674 (1998)
Benzylic zinc reagents add with high regioselectivity to 1- (phenoxycarbonyl) salts derived from pyridine-3-carboxaldehyde (1a) or 3- acetylpyridine (b) to yield 1-(phenoxylcarbonyl)-4-benzyl-1,4- dihydropyridine-3-carboxaldehydes 5a, 5c or ketones 5b, 5d. Aromatizations of these dihydro analogues with sulfur led to the corresponding aldehydes 6a, 6c or ketones 6b, 6d. An alternate synthesis to the aldehydic precursors involved additions of benzylic zinc reagents to 1-(phenoxycarbonyl) salts formed from methyl nicotinates which led to the corresponding methyl 1- (phenoxycarbonyl)-4-benzyl-1,4-dihydronicotinates 7a, 7b. Aromatizations of 7a, 7b led to the corresponding pyridine esters 8a, 8b which on reduction with lithium aluminum hydride yielded the corresponding carbinols 9a, 9b. Oxidation of 9a, 9b by manganese dioxide afforded aldehydes 6e, 6f. Aldehydes 6a-f were readily converted into the benz[g]isoquinolines 10a-f on heating in polyphosphoric acid.
