29538-77-0 Usage
Uses
Used in Pharmaceutical Industry:
(E)-4-Chlorocyclohexanol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its role in this industry is vital, as it aids in the production of essential medicines that cater to diverse health needs.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-4-Chlorocyclohexanol is utilized as a chemical intermediate for the development of products that protect crops from pests and diseases, thereby ensuring increased agricultural productivity.
Used in Dye Industry:
(E)-4-Chlorocyclohexanol is employed as a chemical intermediate in the production of dyes, which are used across various industries for coloring textiles, plastics, and other materials.
Used in Healthcare Industry:
(E)-4-Chlorocyclohexanol is used as an antimicrobial and antifungal agent in the healthcare industry. Its properties make it a valuable component in the development of products that help prevent and treat infections.
Used in Agricultural Industry:
Within the agricultural industry, (E)-4-Chlorocyclohexanol is used for its antimicrobial and antifungal properties, contributing to the development of products that protect crops from diseases and enhance overall crop health.
Check Digit Verification of cas no
The CAS Registry Mumber 29538-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,3 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29538-77:
(7*2)+(6*9)+(5*5)+(4*3)+(3*8)+(2*7)+(1*7)=150
150 % 10 = 0
So 29538-77-0 is a valid CAS Registry Number.
29538-77-0Relevant academic research and scientific papers
Metal-assisted Reactions. Part 17. Ring-opening and Dimerization of Cyclic Ethers by Titanium Halides
Delaney, Paul A.,Johnstone, Robert A. W.,Entwistle, Ian D.
, p. 1855 - 1860 (2007/10/02)
Reaction of TiCl4 or TiBr4 with a variety of cyclic ethers gives, predominantly, products resulting from simple ring-opening or from ring-opening with simultaneous condensation to dimeric species.The variations in yields of these two kinds of products might be correlated qualitatively with an initial formation of the complex TiX4*2E (X = Cl or Br; E = cyclic ether) in which the ethers were held in a cis or trans relationship.Although such a correlation might suggest that TiCl4 but not TiBr4 exerts a template effect on the condensation, stereochemical considerations of the reaction products indicate otherwise.TiCl3 and VCl3 do not give similar results and TiF4 gives no reaction.
