4695-07-2

Basic information

• Product Name: racem.-bis-(phenyl-carboxy-methyl)-disulfide
• CAS NO: 4695-07-2
• Molecular Weight: 334.417
• Mol File: 4695-07-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: racem.-bis-(phenyl-carboxy-methyl)-disulfide(CAS DataBase Reference)
• NIST Chemistry Reference: racem.-bis-(phenyl-carboxy-methyl)-disulfide(4695-07-2)
• EPA Substance Registry System: racem.-bis-(phenyl-carboxy-methyl)-disulfide(4695-07-2)

Safety Data

• Hazardous Substances Data: 4695-07-2(Hazardous Substances Data)

Upstream product

• 4870-65-9 2-bromophenylacetic acid 
• 16201-51-7 (R)-2-mercapto-3-phenylacetic acid (R-thiomandelic acid) 
• 4695-09-4 α-mercaptophenylacetic acid 
• 7505-92-2 2-oxo-2-phenylacetamide 
• 60027-35-2 4-phenyl-1,3,2-oxathiazolylium-5-olate 

Downstream Products

• 103-82-2 phenylacetic acid 
• 611-73-4 Benzoylformic acid 
• 4695-09-4 α-mercaptophenylacetic acid 
• 65-85-0 benzoic acid 

Relevant articles and documents

Thiol-Containing Metallo-β-Lactamase Inhibitors Resensitize Resistant Gram-Negative Bacteria to Meropenem

The prevalence of infections caused by metallo-β-lactamase (MBL) expressing Gram-negative bacteria has grown at an alarming rate in recent years. Despite the fact that MBLs can deactivate virtually all β-lactam antibiotics, there are as of yet no approved

Chiroptical Properties of 2,2'-Dithio- and 2,2'-Diselenobisacetic Acids

Circular dichroism (CD) studies of 2,2'-dithiobisacetic acids substituted with alkyl or phenyl groups and their diselenide analogues show that considerable interaction occurs between the disulfide (or diselenide) chromophore and the carboxyl or phenyl groups, giving rise to intense Cotton effects (CE's) which dominate the near UV region of CD spectrum.In contrast, when the disulfide and carboxyl chromophores are separated by two carbon atoms, each chromophore gives a separate CE of normal intensity at the expected wavelength with no evidence of interaction between them.