37951-47-6 Usage
Description
3-Benzyloxypropiophenone is an organic compound that exists as a colorless oil. It serves as a crucial intermediate in the synthesis of various pharmaceutical products, including ectoparasiticides, drug metabolites, and analgesic agents.
Uses
Used in Pharmaceutical Industry:
3-Benzyloxypropiophenone is used as an intermediate for the production of various ectoparasiticides, which are substances that help in the treatment and prevention of ectoparasites, such as lice and ticks. Its role in the synthesis of these agents is crucial for their effectiveness in controlling and eliminating these parasites.
Additionally, 3-benzyloxypropiophenone is used as an intermediate in the synthesis of drug metabolites. These metabolites are the products of the body's metabolism of drugs, which can sometimes have therapeutic effects or may be inactive or even toxic. 3-benzyloxypropiophenone's involvement in their production is essential for understanding the pharmacokinetics and pharmacodynamics of various medications.
Furthermore, 3-benzyloxypropiophenone is utilized as an intermediate in the creation of analgesic agents, which are substances that help alleviate pain. Its role in the synthesis of these pain-relieving drugs is vital for their effectiveness in providing relief to patients suffering from various types of pain.
Check Digit Verification of cas no
The CAS Registry Mumber 37951-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37951-47:
(7*3)+(6*7)+(5*9)+(4*5)+(3*1)+(2*4)+(1*7)=146
146 % 10 = 6
So 37951-47-6 is a valid CAS Registry Number.
37951-47-6Relevant articles and documents
Studies of the new herbicide KIH-6127. Part II. Synthesis and herbicidal activity of 6-acyl pyrimidin-2-yl salicylates and analogues against barnyard grass
Tamaru,Takehi,Masuyama,Hanai
, p. 327 - 335 (2007/10/03)
The method reported previously (Part I) was employed to prepare a variety of novel 6-acylsalicylates as key intermediates. 6-Acylpyrimidin-2- yl salicylates (2-acyl-6-[(4,6-disubstituted pyrimidin-2-yl)oxy]benzoate derivatives: Type 1), the closely relate