64666-41-7 Usage
Type of compound
Alcohol
It is an organic compound with a hydroxyl (OH) functional group, which gives it its characteristic properties as an alcohol.
Aromatic properties
Commonly used in fragrance production
1-methyl-1H-inden-1-ol has a pleasant, aromatic scent that makes it suitable for use in various fragrances.
Color
Colorless to pale yellow liquid
The compound appears as a colorless to pale yellow liquid, which is typical for many organic compounds.
Odor
Floral and woody
1-methyl-1H-inden-1-ol has a distinct floral and woody odor, which contributes to its use in fragrance production.
Synthesis of pharmaceuticals
Used in the production of pharmaceuticals
The compound can be used as a building block or intermediate in the synthesis of various pharmaceuticals, making it valuable in the pharmaceutical industry.
Synthesis of other organic compounds
Acts as a precursor for the preparation of other chemicals
1-methyl-1H-inden-1-ol can be used as a starting material or intermediate in the synthesis of other organic compounds, making it a versatile building block in the chemical industry.
Applications
Fragrance production, pharmaceutical synthesis, and chemical manufacturing
The compound has a wide range of applications in various industries, including the production of fragrances, synthesis of pharmaceuticals, and manufacturing of other chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 64666-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,6 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64666-41:
(7*6)+(6*4)+(5*6)+(4*6)+(3*6)+(2*4)+(1*1)=147
147 % 10 = 7
So 64666-41-7 is a valid CAS Registry Number.
64666-41-7Relevant articles and documents
Substituent Effect Behavior in the Antiaromatic Inden-1-yl Cation System
Friedrich, Edwin C.,Tam, Teresa M.
, p. 315 - 319 (2007/10/02)
Studies of the rate-accelerating effects in solvolysis produced by 5-methyl and 5-methoxy substituents on the benzene ring and a 3-methyl substituent on the double bond of the inden-1-yl 3,5-dinitrobenzolate system have been carried out.In both 80percent aqueous acetone and in 2,2,2-trifluoroethanol, the rate accelerations observed in the inden-1-yl system were approximately the same as those found in model cyclopenten-3-yl and indan-1-yl systems.From these results, it is concluded that delocalization of charge into both the benzene ring and double bond of the 8?-electron inden-1-yl carbocation is taking place and is apparently undiminished by antiaromatic effects.
