40188-25-8

Basic information

• Product Name: 2,3-Diphenyl-but-3-en-2-yl-hydroperoxide
• Synonyms: 2,3-Diphenyl-but-3-en-2-yl-hydroperoxide
• CAS NO: 40188-25-8
• Molecular Weight: 240.302
• Mol File: 40188-25-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2,3-Diphenyl-but-3-en-2-yl-hydroperoxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Diphenyl-but-3-en-2-yl-hydroperoxide(40188-25-8)
• EPA Substance Registry System: 2,3-Diphenyl-but-3-en-2-yl-hydroperoxide(40188-25-8)

Safety Data

• Hazardous Substances Data: 40188-25-8(Hazardous Substances Data)

Upstream product

• 2510-98-7 2,3-diphenyl-2-butene 
• 782-06-9 (E)-2,3-diphenylbutene 
• 36687-90-8 2-Acetyl-5-(2'-thienylethynyl)thiophene 
• 782-05-8 (Z)-2,3-diphenyl-2-butene 

Downstream Products

• 98-86-2 acetophenone 
• 86939-06-2 2-(1-hydroxyl-1-phenylethyl)-2-phenyloxirane 
• 53116-86-2 1,2-Diphenyl-2-hydroperoxy-1-propanon 
• 86939-05-1 1-Phenyl-1-(3-phenyl-[1,2]dioxetan-3-yl)-eth-1-yl-hydroperoxide 
• 40188-27-0 2,3-Diphenylbut-3-en-2-ol 

Relevant articles and documents

Photochemical approach to the synthesis of naturally occurring thienylacetylenes

Three naturally occurring thienylacetylenes are synthesized through a photochemical coupling of 5-iodo-2-thienyl derivatives and 5-trimethylsilyl-2-thienylacetylene.

Tandem photoarylation-photoisomerization of halothiazoles: Synthesis, photophysical and singlet oxygen activation properties of ethyl 2-arylthiazole-5-carboxylates

The photochemical reaction between ethyl 2-chlorothiazole5-carboxylate and benzene gave no product. In contrast, the reaction with ethyl 2-iodothiazole-5-carboxylate gave ethyl 3-phenylisothiazole-4-carboxylate. The same behaviour was observed if the reac

SYNTHESIS AND PHOTOCHEMICAL PROPERTIES OF NITROTHIENYL DERIVATIVES

Some 2-nitrothienyl derivatives characterized by the presence of an aryl or heteroaryl substituent in the C-5 position were synthesized by using a photochemical coupling procedure.All synthesized compounds were demonstrated to be singlet oxygen sensitizers in the trans-α,α'-dimethylstilbene photooxidation.