928-57-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloroethyl thiocyanate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical properties allow it to be incorporated into the development of new drugs and medications, contributing to advancements in healthcare and medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloroethyl thiocyanate serves as a crucial component in the production of certain agrochemicals. Its application aids in the development of effective pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Used in Chemical Product Manufacturing:
2-Chloroethyl thiocyanate is utilized in the manufacturing of various chemical products, including dyes, plastics, and other specialty chemicals. Its versatility in chemical reactions enables the creation of a wide range of products with diverse applications.
Used in Scientific Research and Development:
The derivatives of 2-Chloroethyl thiocyanate have the potential to be employed in various fields of science and technology. Researchers and scientists explore its properties and reactions to discover new applications and innovations, further expanding its utility in the scientific community.
Due to the toxic nature and potential health hazards of 2-Chloroethyl thiocyanate, it is essential to follow proper handling and disposal methods when working with this chemical to ensure safety and minimize environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 928-57-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 928-57:
(5*9)+(4*2)+(3*8)+(2*5)+(1*7)=94
94 % 10 = 4
So 928-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H4ClNS/c4-1-2-6-3-5/h1-2H2
928-57-4Relevant academic research and scientific papers
Synthesis of six- and seven-membered heterocycles by reaction of 1-(2-chloroethylthio)-1-alkynes and 1-(3-chloropropylthio)-1-alkynes with alkali metal sulfide, selenide and telluride
Sukhai, R. S.,Jong, R. de,Verkruijsse, H. D.,Brandsma, L.
, p. 368 - 372 (2007/10/02)
Reaction of RCC-S-CH2CH2Cl (1, R=alkyl) compounds with dilithium disulfide (Li2S2) in ethanol gives 3-alkyl-5,6-dihydro-1,4-dithiins (2, n=2, X=S).With the alkali monosulfide, M2S, dehydrochlorination to (vinylthio)alkynes RCC-S-CH=CH2 (3) predominates.Interaction between 1, n=2, and M2Se or M2Te (M=Li or Na) in liquid ammonia gives rise to dehydrochlorination as well as to attack on chlorine with intermediate formation of alkynethiolates RCC-S- (4); if this reaction is carried out in ammonia-free ethanol, the desired 5,6-dihydro-1,4-thiaselenins and -thiatellurins (2, n=2, X=Se or Te) are, in some cases, obtained.The chloro sulfides RCC-S-(CH2)3Cl (1, R=alkyl or phenyl) with alkali metal sulfide, selenide and telluride yield respectively 3-alkyl- or 3-aryl-6,7-dihydro-5H-1,4-dithiepins, the corresponding 6,7-dihydro-5H-1,4-thiaselenepins and 6,7-dihydro-5H-thiatellurepins (2, n=3).When R in the starting compounds 2 is a Me3Si group, the unsubstituted compounds 2 (n=3, R=H) are formed.
