41340-31-2 Usage
General Description
6-Methoxytryptophol is a naturally occurring chemical compound that belongs to the family of tryptophan metabolites. It is derived from the amino acid tryptophan and is found in various plant and animal tissues. 6-Methoxytryptophol has been identified as a potential bioactive compound with various physiological and pharmacological activities, including antioxidant, anti-inflammatory, and immunomodulatory effects. It has also been implicated in the regulation of sleep and circadian rhythms. Additionally, 6-Methoxytryptophol has been studied for its potential as a treatment for various neurological disorders. Due to its diverse biological activities, 6-Methoxytryptophol has attracted attention from researchers in the fields of neuroscience, pharmacology, and natural product chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 41340-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,4 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41340-31:
(7*4)+(6*1)+(5*3)+(4*4)+(3*0)+(2*3)+(1*1)=72
72 % 10 = 2
So 41340-31-2 is a valid CAS Registry Number.
41340-31-2Relevant articles and documents
Dearomatization of tryptophols via a vanadium-catalyzed asymmetric epoxidation and ring-opening cascade
Han, Long,Liu, Chuan,Zhang, Wei,Shi, Xiao-Xin,You, Shu-Li
supporting information, p. 1231 - 1233 (2014/02/14)
An enantioselective epoxidation of tryptophols followed by an intramolecular epoxide opening reaction was realized by chiral vanadium catalysts derived from C2 symmetric bis-hydroxamic acid (BHA) ligands. 3a-Hydroxyfuroindoline derivatives with up to 89% yield and 90% ee were obtained under mild reaction conditions.
Convenient Synthesis of 6-Methoxyindole and 6-Methoxytryptophyl Bromide
Feldman, Paul L.,Rapoport, Henry
, p. 735 - 737 (2007/10/02)
A preparatively convenient synthesis of 6-methoxyindole (7) and 6-methoxytryptophylbromide (11) is presented starting with p-cresol (1).Regioselective nitration of p-cresol carbonate (2) followed by hydrolysis of the carbonate and methylation gives 4-methoxy-2-nitrotoluene (5) which is converted to 7 by esterification, reduction and bromination yields 6-methoxytryptophyl bromide (11).The overall yield of 7 and 11 from p-cresol is 43percent and 25percent respectively.
