103122-66-3 Usage
Uses
Used in Pharmaceutical Research and Development:
[(2-Methylpropoxy)thioxomethyl]carbamic acid ethyl ester is used as an intermediate in the pharmaceutical industry for the synthesis of various pharmaceuticals. Its carbamate functional group allows for further chemical reactions and modifications, making it a versatile building block in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, [(2-Methylpropoxy)thioxomethyl]carbamic acid ethyl ester is employed as a key compound for the creation of complex organic molecules. Its unique structure and reactivity enable chemists to explore new reaction pathways and synthesize a wide array of organic compounds with potential applications in various industries.
Used in Agricultural Chemicals:
Although the specific applications are not detailed in the provided materials, [(2-Methylpropoxy)thioxomethyl]carbamic acid ethyl ester may have potential uses in the agricultural chemicals sector. This could include its use as a precursor for the synthesis of pesticides, herbicides, or other agrochemicals that are designed to improve crop yield and protect plants from pests and diseases.
It is crucial to handle and use [(2-Methylpropoxy)thioxomethyl]carbamic acid ethyl ester with caution, as it may pose health and environmental hazards if not properly managed. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, should be taken to minimize any potential risks associated with [(2-Methylpropoxy)thioxomethyl]carbamic acid ethyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 103122-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,2 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103122-66:
(8*1)+(7*0)+(6*3)+(5*1)+(4*2)+(3*2)+(2*6)+(1*6)=63
63 % 10 = 3
So 103122-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO3S/c1-4-11-7(10)9-8(13)12-5-6(2)3/h6H,4-5H2,1-3H3,(H,9,10,13)
103122-66-3Relevant academic research and scientific papers
Preparation of Ethoxycarbonyl Isothiocyanate Using a Pyridine or Quinoline Catalyst
Lewellyn, Morris E.,Wang, Samuel S.,Strydom, Peter J.
, p. 5230 - 5231 (2007/10/02)
A process for the preparation of ethoxycarbonyl isothiocyanate using pyridine or quinoline as a catalyst in an aqueous medium is presented.This process leads to high yields of the desired product with only trace amounts of the thiocyanate being formed.Reaction of ethoxycarbonyl isothiocyanate, prepared in situ, with nucleophiles can be carried out in with yields and purity.
Process for the production of isothiocyanate derivatives
-
, (2008/06/13)
Derivatives of alkoxy, aryloxy and alkene isothiocyanates are produced by the reaction of a haloformate, an alkali, alkaline earth metal, lead or ammonium thiocyanate and a compound having the formula R1 YH wherein R1 is alkyl, aryl or alkoxy, Y is oxygen, sulfur or NR2 and R2 is hydrogen or R1, in the presence of a solvent or water and a catalyst.
