112378-29-7 Usage
Derivative of indole-3-acetic acid
1H-Pyrido[3,4-b]indole-1-acetic acid,
2-benzoyl-2,3,4,9-tetrahydro-9-methyl-, methyl ester is derived from the parent molecule indole-3-acetic acid, which is a naturally occurring organic compound with various biological activities.
Belongs to the class of indoleacetic acids
1H-Pyrido[3,4-b]indole-1-acetic acid,
2-benzoyl-2,3,4,9-tetrahydro-9-methyl-, methyl ester is part of a larger group of organic compounds known as indoleacetic acids, which share a common chemical structure and exhibit various biological activities.
Potential biological activities
1H-Pyrido[3,4-b]indole-1-acetic acid,
2-benzoyl-2,3,4,9-tetrahydro-9-methyl-, methyl ester has been studied for its possible anti-inflammatory, analgesic, and anti-tumor properties, making it a valuable research target for pharmaceutical applications.
Methyl ester form
The presence of a methyl ester group in the compound's structure suggests potential use as a drug delivery agent, which could improve the efficacy and safety of certain medications.
Therapeutic applications
Researchers and pharmaceutical companies are interested in 1H-Pyrido[3,4-b]indole-1-acetic acid,
2-benzoyl-2,3,4,9-tetrahydro-9-methyl-, methyl ester due to its potential therapeutic applications, particularly in the treatment of various diseases and conditions related to inflammation, pain, and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 112378-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,7 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112378-29:
(8*1)+(7*1)+(6*2)+(5*3)+(4*7)+(3*8)+(2*2)+(1*9)=107
107 % 10 = 7
So 112378-29-7 is a valid CAS Registry Number.
112378-29-7Relevant academic research and scientific papers
SYNTHESIS OF 3-(INDOL-2-YL)-PROPENOATE DERIVATIVES OF TRYPTAMINE, VALUABLE INTERMEDIATES FOR THE PREPARATION OF INDOLE ALKALOIDS
Bailey, Patrick D.,Hollinshead, Sean P.
, p. 2879 - 2882 (2007/10/02)
A simple three step route to 3-(indol-2-yl)-propenoate derivatives of tryptamine has been developed, involving the base-induced ring-opening of protected tetrahydro-β-carbolines that result from a modified Pictet-Spengler reaction.
