3185-68-0 Usage
Description
Biphenyl-4-yl chlorothioformate is a chemical compound that features a biphenyl group attached to a chlorothioformate group. It is recognized for its reactivity with alcohols and amines, facilitating the formation of esters and amides, respectively. biphenyl-4-yl chlorothioformate is a versatile reagent in organic synthesis and finds applications across various industries, including pharmaceuticals, agrochemicals, and specialty chemicals. Biphenyl-4-yl chlorothioformate presents as a colorless to light yellow liquid with a distinct pungent odor and is classified as a hazardous chemical, necessitating careful handling.
Uses
Used in Organic Synthesis:
Biphenyl-4-yl chlorothioformate serves as a reagent in organic synthesis, where it is utilized for the formation of esters and amides. Its ability to react with alcohols and amines makes it a valuable component in creating a range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, biphenyl-4-yl chlorothioformate is used as a key intermediate in the synthesis of various drugs. Its role in forming esters and amides is crucial for the development of new medicinal compounds with specific therapeutic properties.
Used in Agrochemical Production:
Biphenyl-4-yl chlorothioformate also finds application in the agrochemical sector, where it contributes to the synthesis of pesticides, herbicides, and other crop protection agents. Its versatility in forming esters and amides aids in the creation of effective and targeted agrochemicals.
Used in Specialty Chemicals:
biphenyl-4-yl chlorothioformate is employed in the production of specialty chemicals, which are tailored for specific industries and applications. Biphenyl-4-yl chlorothioformate's reactivity and functional group compatibility make it suitable for creating unique chemical entities with specialized uses.
Given the compound's hazardous nature, it is imperative that biphenyl-4-yl chlorothioformate is handled with appropriate safety measures to mitigate any potential risks associated with its use in these various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3185-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3185-68:
(6*3)+(5*1)+(4*8)+(3*5)+(2*6)+(1*8)=90
90 % 10 = 0
So 3185-68-0 is a valid CAS Registry Number.
3185-68-0Relevant articles and documents
Oxidative desulfurization-fluorination reaction promoted by [bdmim][F] for the synthesis of difluorinated methyl ethers
Bouvet, Sébastien,Pégot, Bruce,Diter, Patrick,Marrot, Jér?me,Magnier, Emmanuel
, p. 1682 - 1686 (2015/03/14)
A new ionic liquid [bdmim][F] has been prepared and fully characterized. Its potential as a fluoride source for the desulfurization-fluorination process has been evaluated with success. The carbon-sulfur double bond of xanthates and thiocarbonates has bee
A General Synthesis of Very High Specific Activity Tritiomethyl Iodide
Saljoughian, Manouchehr,Morimoto, Hiromi,Williams, Philip G.
, p. 1803 - 1808 (2007/10/02)
A general synthesis of highly tritiated or deuteriated methyl iodide has been elaborated.Tritiodehalogenation of trichloromethyl biphenyl-4-yl ether with tritium gas over Pd/C in ethyl acetate yields the corresponding tritiomethyl biphenyl-4-yl ether of a very high specific activity.Reaction of this product with hydroiodic acid hydrolyses the ether, and quantitatively liberates tritiomethyl iodide.Alkylation of a secondary amine with freshly generated tritiomethyl iodide gives a high yield, and demonstrates the utility of the reagent.Radio-HPLC analysis of the intermediate labelled ether and the amine product showed complete radiochemical purity with full retention of specific activity, and the specificity of labelling was confirmed in both products by 3H NMR spectroscopy.Preparatory chemistry was performed with deuterium gas and the deuteriated reaction products, and analogous analyses performed by HPLC and 2H NMR spectroscopy.
