Recommended Products
Assay
96%
refractive index
n20/D 1.545 (lit.)
bp
72-74 °C/15 mmHg (lit.)
density
1.157 g/mL at 25 °C (lit.)
SMILES string
Fc1ccc(CS)cc1
InChI
1S/C7H7FS/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
InChI key
RKTRHMNWVZRZJQ-UHFFFAOYSA-N
General description
4-Fluorobenzyl mercaptan undergoes reaction with p-chloranil to afford mainly 2,5-dichloro-3,6-S-disubstituted benzoquinone and 2,6-dichloro-3,5-S-disubstituted benzoquinone.
Application
4-Fluorobenzyl mercaptan may be used in the synthesis of the degradation products of fluorapacin, namely bis(4-fluorobenzyl)disulfide and bis(4-fluorobenzyl)tetrasulfide.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
170.0 °F - closed cup
Flash Point(C)
76.67 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Journal of pharmaceutical and biomedical analysis, 48(3), 664-671 (2008-08-06)
Bis(4-fluorobenzyl)trisulfide, fluorapacin, has been extensively developed as a promising new anticancer drug candidate. Its degradation products were identified and verified by the newly synthesized compounds bis(4-fluorobenzyl)disulfide (A) and bis(4-fluorobenzyl)tetrasulfide (B) which were resulted from the disproportionation of fluorapacin under forced
The synthesis of new cyclic thioquinone derivatives.
Heteroatom Chem., 21(6), 446-452 (2010)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service