36865-43-7 Usage
Uses
Used in Pharmaceutical Industry:
1-Chloro-4-ethoxybutane is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing medications.
Used in Agrochemical Industry:
1-Chloro-4-ethoxybutane is used as a chemical intermediate in the production of agrochemicals, aiding in the creation of effective pesticides and other agricultural chemicals to protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
1-Chloro-4-ethoxybutane is utilized as a reagent in organic synthesis, enabling the formation of complex organic molecules and facilitating various chemical reactions.
Used as a Solvent in Industrial Processes:
1-Chloro-4-ethoxybutane is employed as a solvent in a range of industrial processes, including the manufacturing of chemicals, plastics, and other materials, due to its ability to dissolve a wide array of substances.
Check Digit Verification of cas no
The CAS Registry Mumber 36865-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,6 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36865-43:
(7*3)+(6*6)+(5*8)+(4*6)+(3*5)+(2*4)+(1*3)=147
147 % 10 = 7
So 36865-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13ClO/c1-2-8-6-4-3-5-7/h2-6H2,1H3
36865-43-7Relevant academic research and scientific papers
ON THE MECHANISM OF SELECTIVE CHLORINATION OF ETHERS WITH SULFURYL CHLORIDE IN THE DARK
Buyck, Laurent De,Pooter, Herman De
, p. 807 - 816 (2007/10/02)
Alkyl 4-chlorobutyl ethers reacted in the dark with an excess of sulfuryl chloride at 70-85 deg C (bath) to afford α,β,β-trichlorinated ethers.The reactions were accelerated 3- to 6-fold by N,N-dimethyloctylammonium salts (0,12 to 1 mmol/mol ether).This catalyst promoted decomposition of sulfuryl chloride to chlorine and sulfur dioxide and thereby caused serious loss of sulfuryl chloride.The proportions of chlorination at α or α1 position were identical in the catalyzed or uncatalyzed version and depended on inductive effects, correlating well with Taft's linear free energy relationship log k/kref=ρ*?* for R = H, Me, Et, Pr in RCH2O(CH2)4Cl with ρ* = -2.6 +/- 0.1.The overall reactivity of ethers appears to vary like the nucleophilicity of the ether oxygen.It is concluded that hydride abstraction occurs indirectly, probably involving a chloroxonium ion pair.
