188928-11-2 Usage
Description
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol is a white solid compound that serves as a key intermediate in the synthesis of various organic compounds. Its unique structure, featuring a dichloro-substituted benzyloxy group attached to a phenylethanol moiety, makes it a versatile building block for the development of pharmaceuticals and other specialty chemicals.
Uses
Used in Pharmaceutical Industry:
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol is used as a precursor for the preparation of S-[(benzyloxyphenyl)alkyl]isothiourea derivatives, which are known as inhibitors of the Na+-Ca2+ exchanger. These derivatives have potential applications in the treatment of various cardiovascular diseases, as they can help regulate the exchange of sodium and calcium ions across cell membranes, thereby influencing cellular functions and physiological processes.
As a versatile intermediate, 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol can also be utilized in the synthesis of other bioactive compounds and pharmaceutical agents, contributing to the development of new drugs and therapies for various medical conditions. Its chemical properties and structural features make it a valuable component in the design and synthesis of novel molecules with potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 188928-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,2 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188928-11:
(8*1)+(7*8)+(6*8)+(5*9)+(4*2)+(3*8)+(2*1)+(1*1)=192
192 % 10 = 2
So 188928-11-2 is a valid CAS Registry Number.
188928-11-2Relevant articles and documents
Design, synthesis and anti-tubercular evaluation of new 2-acylated and 2-alkylated amino-5-(4-(benzyloxy)phenyl)thiophene-3-carboxylic acid derivatives. Part 1
Lu, Xiaoyun,Wan, Baojie,Franzblau, Scott G.,You, Qidong
experimental part, p. 3551 - 3563 (2011/10/19)
A series of 2-acylated and 2-alkylated amino-5-(4-(benzyloxy)phenyl) thiophene-3-carboxylic acid derivatives were synthesized and evaluated for anti-tubercular activity. Among these compounds, 10d, 15, 12h and 12k inhibited Mycobacterium tuberculosis (Mtb
