54481-26-4

Basic information

• Product Name: diethyl 2,2'-dithiobisbenzoate
• Synonyms: diethyl 2,2'-dithiobisbenzoate;2,2'-Dithiobis(benzoic acid ethyl) ester;2,2'-Dithiodi(benzoic acid ethyl) ester
• CAS NO: 54481-26-4
• Molecular Formula: C₁₈H₁₈O₄S₂
• Molecular Weight: 362.46312
• EINECS: 259-181-1
• Mol File: 54481-26-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: diethyl 2,2'-dithiobisbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2,2'-dithiobisbenzoate(54481-26-4)
• EPA Substance Registry System: diethyl 2,2'-dithiobisbenzoate(54481-26-4)

Safety Data

• Hazardous Substances Data: 54481-26-4(Hazardous Substances Data)

Upstream product

• 19602-82-5 2,2'-dithiodibenzoic acid dichloride 
• 64-17-5 ethanol 
• 147-93-3 Thiosalicylic acid 
• 119-80-2 2,2'-dithiobenzoic acid 
• 658702-69-3 N-[(2-ethoxycarbonylbenzene)sulfenyl]benzimidazole 
• 917-64-6 methyl magnesium iodide 
• 1829-28-3 ethyl 2-iodobenzoate 
• 5651-35-4 2-phenylbenzo[d]-1,3-oxathiin-4-one 
• 141-52-6 sodium ethanolate 

Downstream Products

• 33441-56-4 ethyl 2-mercaptobenzoate 
• 1402735-08-3 methyl 2-((5-(2-hydroxyphenyl)-1,3,4-oxadiazol-2-yl)disulfanyl)benzoate 
• 1402735-05-0 ethyl 2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)disulfanyl)benzoate 
• 1402734-67-1 ethyl 2-((1,3,4-thiadiazol-2-yl)disulfanyl)benzoate 
• 1402734-98-8 ethyl 2-((5-(pyridin-3-yl)-1,3,4-oxadiazol-2-yl)disulfanyl) benzoate 
• 1402734-93-3 ethyl 2-((5-phenyl-1,3,4-oxadiazol-2-yl)disulfanyl)benzoate 
• 1402735-09-4 ethyl 2-((5-(2-hydroxyphenyl)-1,3,4-oxadiazol-2-yl)disulfanyl)benzoate 
• 1441-80-1 o-Chlormercapto-benzoesaeureaethylester 
• 1421695-57-9 C₁₇H₁₁Br₂NO₄S 
• 1421695-55-7 C₁₇H₁₂BrNO₄S 
• 1421695-53-5 C₁₇H₁₂ClNO₄S 
• 1421695-49-9 C₁₇H₁₃NO₄S 

Relevant articles and documents

A novel pathway for the thermolysis of N-nitrosoanthranilates using flash vacuum pyrolysis leading to 7-aminophthalides

Flash vacuum pyrolysis of methyl N-methyl-N-nitrosoanthranilate leads to elimination of nitric oxide and disproportionation of the formed N-radical to 7-(methylamino)phthalide and methyl N-methylanthranilate. This transformation was found to be a convenient, solvent-free method for the preparation of 7-(methylamino)phthalides. An alternative route through pyrolysis of N-benzyl-N-methyl anthranilates was also investigated. This journal is

Synthesis and biological evaluation of nonsymmetrical aromatic disulfides as novel inhibitors of acetohydroxyacid synthase

46 Novel nonsymmetrical aromatic disulfides containing [1,3,4]thiadiazole or [1,3,4]oxadiazole groups were synthesized and their biological activities were evaluated as inhibitors of acetohydroxyacid synthase (AHAS, EC 2.2.1.6). Besides their strong in vitro inhibition against plant AHAS, compounds 3e and 3f also display 80-100% post-emergence herbicidal activities in greenhouse bioassay at 1500 g/ha dosage. The assay of exogenous branched-chain amino acids supplementation on rape root growth of 3e suggests that the herbicidal activity has relationship with AHAS inhibition.

N-(2-Alkoxycarbonylbenzenesulfeny)benzimidazoles as nitrogen-, sulfur-, and carbon-sulfenylation reagents

N-(2-Alkoxycarbonylbenzenesulfenyl)benzimidazoles reacted with nucleophiles such as amides, imidates, thiols, Grignard reagents, and active methylene compounds to yield the corresponding sulfenylated products: N-acylsulfenamides, N-sulfenylimidates, disulfides, sulfides, and sulfenylated active methylene compounds, respectively.