63237-19-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-Aminophenyl)-4-hydroxybutan-1-one is used as an intermediate in the synthesis of paracetamol, a widely recognized medication for reducing pain and fever. Its presence in the production process is crucial for creating an effective and widely accessible remedy for various ailments.
Used in Dye Production:
In the dye industry, 1-(4-Aminophenyl)-4-hydroxybutan-1-one serves as a key component in the creation of various dyes. Its chemical properties allow for the development of a range of colorants used in different applications.
Used in Hair Dye Industry:
1-(4-Aminophenyl)-4-hydroxybutan-1-one is utilized as a component in hair dyes, contributing to the coloration and staining process of hair care products. Its role is essential for achieving the desired color outcomes in hair dye formulations.
Used in Photographic Development:
In the field of photography, 1-(4-Aminophenyl)-4-hydroxybutan-1-one is employed in the production of photographic developers. It aids in the chemical reactions necessary for the development of images on photographic film or paper.
Check Digit Verification of cas no
The CAS Registry Mumber 63237-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,3 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63237-19:
(7*6)+(6*3)+(5*2)+(4*3)+(3*7)+(2*1)+(1*9)=114
114 % 10 = 4
So 63237-19-4 is a valid CAS Registry Number.
63237-19-4Relevant articles and documents
Investigation of some basic propyl(alkyl) phenyl ketones with local anesthetic activity
Rudinger Adler,Buechi
, p. 544 - 551 (2007/10/05)
The authors synthetised several ketone analogues of procaine (II) with different lipophilic substituents (XVI). In order to investigate structure-activity relationship, the Rm values (measure for the partition coefficient), the -CO- wave frequency (expression of electron density) and the local anesthetic activity (rabbit cornea) were determined. The studied lipophilic substituents do not influence the inductive or mesomeric effect on the carbonyl oxygen and so do not increase its electron density. On the other hand, they do increase the partition coefficient, therefore the hydrophobic binding effect of the substituents is improved. The lower efficacy of the carbonyl group in ketones against the carboxyl group can be compensated for by introduction of groups with higher liposolubility, so that even in ketones it is possible to prepare substances with high local-anesthetic activity.
