54584-24-6 Usage
General Description
2-Methylbenzofuran-6-ol, also known as 2-methyl-6-benzofuranol, is a chemical compound with a unique aromatic and woody odor. It is commonly used in the fragrance and flavor industry for its pleasant scent, resembling that of sandalwood. 2 - Methylbenzofuran - 6 - ol is found in natural sources such as agarwood, and it also serves as a pheromone in some insect species. Additionally, 2-Methylbenzofuran-6-ol has been studied for its potential antimicrobial and antioxidant properties. As a result, it is used in various cosmetic and personal care products as a fragrance ingredient and for its potential beneficial effects on skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 54584-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54584-24:
(7*5)+(6*4)+(5*5)+(4*8)+(3*4)+(2*2)+(1*4)=136
136 % 10 = 6
So 54584-24-6 is a valid CAS Registry Number.
54584-24-6Relevant articles and documents
The reaction of arylacetones with boron tribromide
Dupont, Romain,Cotelle, Philippe
, p. 1651 - 1655 (1999)
Treatment of arylacetones 1 with boron tribromide gives 1,3-dimethyl-2- arylnaphthalenes 3 in fair to good yields by a tandem aldol condensation- intramolecular cyclization. This reaction is limited to the electron-rich arylacetones. In the case of methox
COMPOUNDS AND METHODS FOR MODULATING FXR
-
Page/Page column 27, (2008/06/13)
Compounds of formula. wherein variables are as defined herein and their pharmaceutical compositions and methods of use are disclosed as useful for treating dyslipidemia and related diseases.
Facile construction of the benzofuran and chromene ring systems via Pd II-catalyzed oxidative cyclization
So, Won Youn,Jeong, Im Eom
, p. 3355 - 3358 (2007/10/03)
(Chemical Equation Presented) We herein report the development of one-pot procedures for the conversion of allyl aryl ethers to 2-methylbenzofurans (via sequential Claisen rearrangement and oxidative cyclization) and for the conversion of aryl homoallyl e
