1591-43-1 Usage
Description
1-(4-Chlorobenzyl)naphthalene, also known as 4-chlorobenzyl naphthalene, is a chemical compound that features a naphthalene core with a 4-chlorobenzyl group attached to it. This white to off-white solid is sparingly soluble in water but more soluble in organic solvents, making it a versatile compound for various applications.
Uses
Used in Fragrance Industry:
1-(4-Chlorobenzyl)naphthalene is used as a fragrance ingredient for its distinct scent, contributing to the creation of various fragrances in the perfumery and cosmetic industries.
Used in Consumer Product Manufacturing:
It is also utilized in the manufacturing of consumer products such as soaps, detergents, and personal care items, enhancing their fragrance and appeal to consumers.
Used in Pharmaceutical Research:
1-(4-Chlorobenzyl)naphthalene is used as a potential cancer preventive agent in pharmaceutical research due to its ability to inhibit the growth of cancer cells. Its study is ongoing to explore its full potential in cancer treatment and prevention.
It is crucial to handle 1-(4-Chlorobenzyl)naphthalene with care, as improper use may lead to harmful effects. Its applications span across the fragrance, consumer product, and pharmaceutical industries, showcasing its versatility and potential impact on these sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 1591-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1591-43:
(6*1)+(5*5)+(4*9)+(3*1)+(2*4)+(1*3)=81
81 % 10 = 1
So 1591-43-1 is a valid CAS Registry Number.
1591-43-1Relevant articles and documents
The nitromethane initiator of the Friedel-Crafts naphthalene reaction using microwaves
Bratulescu,Le Bigot,Delmas
, p. 3309 - 3313 (2001)
The alkylation of naphthalene using halogen derivatives may be achieved under very simple conditions by the Friedel-Crafts reaction. The products are obtained by irradiation of the paste containing the reaction mixture and a small quantity of nitromethane to initiate the reaction.
Efficient N-heterocyclic carbene nickel pincer complexes catalyzed cross coupling of benzylic ammonium salts with boronic acids
Liu, Xi-Yu,Zhu, Hai-Bo,Shen, Ya-Jing,Jiang, Jian,Tu, Tao
, p. 350 - 353 (2017/01/28)
Pyridine-bridged bis-benzimidazolylidene nickel complexes exhibited very high catalytic activity toward cross coupling of inactive (hetero)aryl benzylic ammonium salts with (hetero)aryl and alkenyl boronic acids under mild reaction conditions. Even at 2 mol% catalyst loading, a wide range of substrates for both coupling partners with different steric and electronic properties were well tolerated.
Thermal Fragmentation Reactions of Dihydroaromatic Molecules
Miller, Bernard,Shi, Xiaolian,Grosu, George,Zhou, Renmo
, p. 2320 - 2323 (2007/10/02)
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