745784-02-5 Usage
Uses
Used in Organic Synthesis:
(S)-(-)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is used as a reagent in organic synthesis for the preparation of various organic compounds. Its unique structure allows it to be a versatile building block in the creation of new molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (S)-(-)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is used as a key intermediate in the development of new drugs. Its properties make it a valuable component in the synthesis of potential therapeutic agents.
Used in Agrochemicals:
(S)-(-)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is also utilized in the agrochemical sector, where it serves as a reagent in the synthesis of compounds used for pest control and crop protection.
Used in Materials Science Research:
(S)-(-)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE contributes to the field of materials science by being a component in the research and development of new materials with specific properties.
Used in Biochemistry:
(S)-(-)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE has potential applications in biochemistry, particularly in the study of protein interactions and modifications, where its unique structure can provide insights into biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 745784-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,7,8 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 745784-02:
(8*7)+(7*4)+(6*5)+(5*7)+(4*8)+(3*4)+(2*0)+(1*2)=195
195 % 10 = 5
So 745784-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrNS/c1-7(11-6-12)8-2-4-9(10)5-3-8/h2-5,7H,1H3/t7-/m0/s1
745784-02-5Relevant academic research and scientific papers
Electrochemical Benzylic C(sp3)-H Isothiocyanation
Guo, Weisi,Li, Ming,Li, Yufeng,Wang, Tao,Wen, Lirong,Zhang, Shanxue
supporting information, p. 1742 - 1746 (2022/03/14)
Selective C(sp3)-H isothiocyanation represents a significant strategy for the synthesis of isothiocyanate derivatives. We report herein an electrochemical benzylic isothiocyanation in a highly chemo- and site-selective manner under external oxidant-free conditions. The high chemoselectivity is attributed to the facile in situ isomerization of benzylic thiocyanates to isothiocyanates. Notably, the method exhibits high functional group compatibility and is suitable for late-stage functionalization of bioactive molecules.
Synthesis and spectroscopic analysis of substituted 2-aminothiazolines
Ferreira, Renan B.,Tormena, Claudio F.,Almeida, Wanda P.
, p. 186 - 190 (2013/05/22)
2-Aminothiazolines can exist in two tautomeric species, amino and imino forms, which can theoretically exist as two stereoisomers. Several methods and techniques have been used to evaluate tautomeric process, but in this case 15N NMR spectrosco
