19552-10-4 Usage
Description
4-BROMOBENZYL MERCAPTAN is an organic compound characterized by the presence of a bromine atom at the para position of a benzyl group, which is connected to a thiol (mercaptan) group. This unique structure endows it with specific chemical properties that make it suitable for various applications in different industries.
Uses
Used in Chemical Synthesis:
4-BROMOBENZYL MERCAPTAN is used as a synthetic intermediate for the production of various organic compounds. Its ability to undergo desulfurization reactions makes it a valuable precursor in the synthesis of other molecules.
Used in Pharmaceutical Industry:
4-BROMOBENZYL MERCAPTAN is used as a building block for the development of pharmaceutical compounds. Its unique structure can be exploited to create new drugs with potential therapeutic applications.
Used in Chemical Research:
4-BROMOBENZYL MERCAPTAN serves as a research tool in the field of organic chemistry. It can be used to study the reactivity of different functional groups and to develop new synthetic methodologies.
Used in the Synthesis of 4-Bromotoluene:
4-BROMOBENZYL MERCAPTAN is used as a starting material for the synthesis of 4-bromotoluene via desulfurization with molybdenum hexacarbonyl [Mo(CO)6] in tetrahydrofuran. This reaction is an example of its utility in chemical synthesis, particularly in the production of substituted aromatic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 19552-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19552-10:
(7*1)+(6*9)+(5*5)+(4*5)+(3*2)+(2*1)+(1*0)=114
114 % 10 = 4
So 19552-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrS/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
19552-10-4Relevant articles and documents
SULFUR EXTRUSION FROM DISULFIDES BY CARBENES
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Page/Page column 19, (2021/10/30)
The present invention relates to a method for preparing a compound T having a thioether group from a compound D having a disulfide group in the presence of a carbene.
Nonenzymatic Dynamic Kinetic Resolution of in situ Generated Hemithioacetals: Access to 1,3-Disubstituted Phthalans
Nath, Utpal,Chowdhury, Deepan,Pan, Subhas Chandra
supporting information, p. 1628 - 1633 (2018/03/21)
The first nonenzymatic DKR reaction of hemithioacetals is developed. Hemithioacetals were formed in situ via thiol addition and subsequently underwent an intramolecular oxa-Michael reaction. The scope of the reaction was quite broad ranging from aliphatic to aromatic substituents and 1,3-disubstituted-1,3-dihyroisobenzofuran products were obtained in good yields with moderate diastereoselectivities and high enantioselectivities. (Figure presented.).
Preparation and in-vitro evaluation of 4-benzylsulfanylpyridine-2- carbohydrazides as potential antituberculosis agents
Herzigova, Petra,Klimesova, Vera,Palat, Karel,Kaustova, Jarmila,Dahse, Hans-Martin,Moellmann, Ute
body text, p. 394 - 404 (2009/11/30)
A set of 4-benzylsulfanylpyridine-2-carbohydrazides was synthesized and evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, non-tuberculous mycobacteria, and multidrug-resistant M. tuberculosis. The activities expressed as the minimum inhibitory concentration (MIC) fall into a range of 2 to 125 μmol/L, most often 4 to 32 μmol/L. The results revealed that the substituents on the benzyl moiety do not influence the antimycobacterial efficacy. The substances exhibited similar activities against sensitive and resistant strains of M. tuberculosis. Furthermore, compounds show low antiproliferative effect and cytotoxicity.
