6326-56-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(1-hydroxynaphthalen-2-yl)butan-1-one is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Dye and Pigment Industry:
1-(1-hydroxynaphthalen-2-yl)butan-1-one is used as a starting material for the production of dyes and pigments. Its chemical properties make it suitable for creating a wide range of colors and shades, contributing to the diversity of products in this industry.
Used in Fragrance Industry:
1-(1-hydroxynaphthalen-2-yl)butan-1-one is used as a base for creating various fragrances. Its distinct chemical structure enables the development of unique and complex scents, adding value to the fragrance industry.
Check Digit Verification of cas no
The CAS Registry Mumber 6326-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6326-56:
(6*6)+(5*3)+(4*2)+(3*6)+(2*5)+(1*6)=93
93 % 10 = 3
So 6326-56-3 is a valid CAS Registry Number.
6326-56-3Relevant academic research and scientific papers
Ytterbium triflate catalysed Friedel-Crafts reaction using carboxylic acids as acylating reagents under solvent-free conditions
Jin, Can,Li, Jie,Su, Weike
experimental part, p. 607 - 611 (2011/02/26)
The Friedel-Crafts acylation of 1-naphthol and phenol derivatives with carboxylic acids were investigated by using a catalytic amount of metal-triflate, in particular Yb(OTf)3, under solvent-free conditions. Both aliphatic and aromatic carboxylic acids reacted easily to afford the corresponding hydroxyaryl ketones.
Solvent affected facile synthesis of hydroxynaphthyl ketones: Lewis acids promoted Friedel-Crafts and demethylation reaction
Li, Wan-Mei,Lai, Hu-Qin,Ge, Zhong-Hua,Ding, Cheng-Rong,Zhou, Ying
, p. 1595 - 1601 (2008/02/01)
Hydroxynaphthyl ketones were obtained with high yields under very mild conditions in the presence of AlCl3 via Friedel-Crafts acylation and demethylation from naphthyl ethers. Several Lewis acids were tested, and AlCl3 was the most efficient catalyst. Copyright Taylor & Francis Group, LLC.
