42068-67-7 Usage
Uses
Used in Chemical Synthesis:
S-2-PROPEN-1-YL ESTER CARBONOCHLORIDOTHIOIC ACID is used as an intermediate in the synthesis of various organic compounds due to its reactivity and the presence of the thioate functional group.
Used in Pesticide and Herbicide Production:
In the Agrochemical Industry, S-2-PROPEN-1-YL ESTER CARBONOCHLORIDOTHIOIC ACID is used as a key component in the production of pesticides and herbicides, contributing to their effectiveness in controlling unwanted plant and insect species.
Used in Antimicrobial and Antifungal Applications:
S-2-PROPEN-1-YL ESTER CARBONOCHLORIDOTHIOIC ACID is used as an antimicrobial and antifungal agent for its potential to inhibit the growth of microorganisms, making it a candidate for applications in sanitization and preservation processes.
Safety Precautions:
It is important to handle S-2-PROPEN-1-YL ESTER CARBONOCHLORIDOTHIOIC ACID with care, as it is toxic and can cause irritation to the skin, eyes, and respiratory system upon contact or inhalation. Proper safety measures, including the use of personal protective equipment and handling in well-ventilated areas, should be taken to minimize exposure risks.
Check Digit Verification of cas no
The CAS Registry Mumber 42068-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42068-67:
(7*4)+(6*2)+(5*0)+(4*6)+(3*8)+(2*6)+(1*7)=107
107 % 10 = 7
So 42068-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H5ClOS/c1-2-3-7-4(5)6/h2H,1,3H2
42068-67-7Relevant academic research and scientific papers
CHLOROTHIOFORMATE MANUFACTURING METHOD
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Page/Page column 3, (2011/10/19)
The present invention relates to a process for producing chlorothioformate comprising reacting an alkenyl mercaptan with phosgene in a reactor in the presence of a carboxylic acid amide in an organic solvent, characterized in that the carboxylic acid amide is preliminary charged to the reactor in an amount of 10 to 50% by weight based on the whole amount of the carboxylic acid amide, and subsequently, the compound of the formula (I), phosgene and the remaining carboxylic acid amide are charged to the reactor.
S-alkyl chlorothioformates from xanthates
Gade, Alexandra M.,Abelt, Christopher J.
, p. 2097 - 2099 (2008/02/12)
Reaction of S-alkyl O-ethyl xanthates (S-alkyl O-ethyl dithiocarbonates) with catalytic Vilsmeier reagent generated in situ from N-formylmorpholine (morpholine-4-carbaldehyde) gives S-alkyl chlorothioformates in good yields. Georg Thieme Verlag Stuttgart.
Rapid [3,3] sigmatropic rearrangements of allylic thiono chloroformates
Zaim, Oemer
, p. 8059 - 8062 (2007/10/03)
Treatment of allylic alcohols with thiophosgene and pyridine gives thiolo chloroformates directly at room temperature, presumably via very rapid [3,3] sigmatropic rearrangements of thiono chloroformates. Synthesis of allyl thiono chloroformate from allyl alcohol, sodium hydride and thiophosgene at low temperature and warming up to room temperature supports this finding.
