Cas 58380-03-3,(E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione

58380-03-3

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Basic information

Product Name: (E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione
Synonyms: (E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione
CAS NO:58380-03-3
Molecular Formula:
Molecular Weight: 266.299
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione(58380-03-3)
EPA Substance Registry System: (E)-1-phenyl-2-(2-phenylhydrazono)butane-1,3-dione(58380-03-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 58380-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 58380-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,8 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58380-03:
(7*5)+(6*8)+(5*3)+(4*8)+(3*0)+(2*0)+(1*3)=133
133 % 10 = 3
So 58380-03-3 is a valid CAS Registry Number.

58380-03-3Upstream product

58380-03-3Downstream Products

58380-03-3Relevant academic research and scientific papers

Pyridine-Catalysed Desulfonylative Addition of β-Diketones to Arylazosulfones via Diaziridine Rearrangement

Ji, Xin,Meng, Ling-Guo,Xu, Hailong,Wang, Lei

supporting information, p. 1142 - 1146 (2020/12/31)

A pyridine-catalysed desulfonylative addition of β-diketones to arylazosulfones was developed to obtain diazenyl β-dicarbonyl compounds. The aryldiazenyl group was observed in the desired product from arylazosulfones, and this diazenylation reaction was achieved via a possible rearrangement process based on diaziridine ring cleavage. The scope of the protocol was investigated and a plausible mechanism was given. (Figure presented.).

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