16519-20-3 Usage
Description
[(heptyloxy)methyl]benzene, also known as heptyloxymethylbenzene, is an organic compound with the molecular formula C16H26O. It is classified as an alkylbenzene and is composed of a benzene ring with a heptyloxymethyl group attached to it. [(heptyloxy)methyl]benzene is characterized by its sweet, aromatic odor, making it a valuable ingredient in the fragrance industry.
Uses
Used in Fragrance Industry:
[(heptyloxy)methyl]benzene is used as a fragrance ingredient for its sweet, aromatic odor. It is particularly suitable for the production of perfumes and other scented products, adding a pleasant and distinctive scent to these items.
Used in Personal Care Products:
In the personal care industry, [(heptyloxy)methyl]benzene is used as a fragrance component in various products such as lotions, creams, and shampoos. Its sweet, aromatic scent enhances the overall sensory experience of these products, making them more appealing to consumers.
Used in Household Cleaning Products:
[(heptyloxy)methyl]benzene is also utilized in the formulation of household cleaning products, where its pleasant aroma helps to mask unpleasant odors and provide a fresh, clean scent to the environment.
Used as a Precursor in Organic Chemistry:
[(heptyloxy)methyl]benzene serves as an important intermediate in organic chemistry, being used as a precursor in the synthesis of various organic compounds. Its versatile chemical structure allows for further modification and functionalization, making it a valuable building block in the development of new molecules with potential applications in various industries.
Overall, [(heptyloxy)methyl]benzene is a versatile chemical with a wide range of applications in the fragrance, personal care, household cleaning, and organic chemistry industries, primarily due to its sweet, aromatic odor and its utility as a synthetic intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 16519-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,1 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16519-20:
(7*1)+(6*6)+(5*5)+(4*1)+(3*9)+(2*2)+(1*0)=103
103 % 10 = 3
So 16519-20-3 is a valid CAS Registry Number.
16519-20-3Relevant articles and documents
Synthesis of Benzyl Alkyl Ethers by Intermolecular Dehydration of Benzyl Alcohol with Aliphatic Alcohols under the Effect of Copper Containing Catalysts
Bayguzina,Gimaletdinova,Khusnutdinov
, p. 1148 - 1155 (2018/10/24)
Synthesis of benzyl alkyl ethers was performed in high yields by intermolecular dehydration of benzyl and primary, secondary, tertiary alcohols under the effect of copper containing catalysts. The formation of benzyl alkyl ethers occurs with participation of benzyl cation.
Organohalide-catalyzed dehydrative O-alkylation between alcohols: A facile etherification method for aliphatic ether synthesis
Xu, Qing,Xie, Huamei,Chen, Pingliang,Yu, Lei,Chen, Jianhui,Hu, Xingen
supporting information, p. 2774 - 2779 (2015/05/27)
Organohalides are found to be effective catalysts for dehydrative O-alkylation reactions between alcohols, providing selective, practical, green, and easily scalable homo- and cross-etherification methods for the preparation of useful symmetrical and unsymmetrical aliphatic ethers from the readily available alcohols. Mechanistic studies revealed that organohalides are regenerated as reactive intermediates and recycled to catalyze the reactions.
A novel method for synthesis of benzyl alkyl ethers using Vanadium-based metal complex catalysts
Khusnutdinov,Bayguzina,Gallyamova,Dzhemilev
, p. 261 - 266 (2012/10/29)
A novel method has been developed for the synthesis of benzyl alkyl ethers in 25-85% yields via the reaction of toluene with alcohols in a CCl4 medium catalyzed by Et3N-activated VO(acac)2.