78575-06-1 Usage
Uses
Used in Food Industry:
4-isopropylbutyrophenone is used as a flavor additive for its aromatic and sweet smell, reminiscent of raspberries, enhancing the taste and aroma of food products.
Used in Cosmetic Industry:
4-isopropylbutyrophenone is used as a fragrance additive in perfumes, soaps, and lotions, providing a pleasant and appealing scent to cosmetic products.
Used in Pharmaceutical Industry:
4-isopropylbutyrophenone is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of various medicinal compounds.
Used in Agrochemical Industry:
4-isopropylbutyrophenone is used as an intermediate in the synthesis of agrochemicals, aiding in the production of agricultural products and chemicals.
Used in Polymer and Plastics Production:
4-isopropylbutyrophenone has applications in the production of polymers and plastics, playing a role in the manufacturing process of these materials.
Due to its low toxicity, 4-isopropylbutyrophenone is considered safe for use in consumer products across these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 78575-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78575-06:
(7*7)+(6*8)+(5*5)+(4*7)+(3*5)+(2*0)+(1*6)=171
171 % 10 = 1
So 78575-06-1 is a valid CAS Registry Number.
78575-06-1Relevant academic research and scientific papers
Facile preparation of 5-alkyl-1-aryltetrazoles with arenes, acyl chlorides, hydroxylamine, and diphenylphosphoryl azide
Shibasaki, Kaho,Togo, Hideo
, p. 1816 - 1830 (2020/11/19)
Successive treatment of arenes with acyl chlorides and AlCl3, the addition of water and removal of solvent, the reaction with NH2OH?HCl and K2CO3, and the reaction with diphenylphosphoryl azide and DBU under warming conditions gave the corresponding 5-alkyl-1-aryltetrazoles efficiently in good to moderate yields. The present method is one-pot transformation of arenes into 5-alkyl-1-aryltetrazoles using the Friedel-Crafts acylation and the Beckmann rearrangement under transition-metal-free conditions.
