Cas 262296-58-2,1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one

262296-58-2

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Basic information

Product Name: 1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one
Synonyms: 1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one
CAS NO:262296-58-2
Molecular Formula:
Molecular Weight: 238.289
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: 1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one(262296-58-2)
EPA Substance Registry System: 1-p-Tolyl-3,3a-dihydro-1H-cycloheptaimidazol-2-one(262296-58-2)

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: 262296-58-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 262296-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,2,9 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 262296-58:
(8*2)+(7*6)+(6*2)+(5*2)+(4*9)+(3*6)+(2*5)+(1*8)=152
152 % 10 = 2
So 262296-58-2 is a valid CAS Registry Number.

262296-58-2Upstream product

262296-58-2Downstream Products

3716-19-6 N-(p-methylphenyl)-1,3-diazaazulanone

262296-58-2Relevant academic research and scientific papers

Electrochemical oxidations of 1,3'dihydro-1,3-diazaazulanones and effects of reaction temperature

Saito, Katsuhiro,Ueda, Yosuke,Kawamura, Ayako,Kajita, Akiyoshi,Ishiguro, Hiroyuki,Ido, Takayasu,Ono, Katsuhiko,Awadu, Yasutaka

, p. 63 - 70 (2007/10/03)

Electrochemical oxidations of 1-tosyl-3-aryl-1,3-dihydro-1,3'diazaazulanones at 0°C afforded 3-aryl-6-tosyl-1,3-dihydro-1,3-diazaazulanones via migrations of the tosyl group. However, the same type of electrochemical oxidations at an elevated temperature

Electrochemistry of 1,3-diazadihydroazulanone: Electrochemical reduction and oxidation of 1-tosyl-3-aryl-1,3-diazadihydroazulanone leading to migration and elimination of the tosyl group

Saito, Katsuhiro,Ido, Takayasu,Awadu, Yasutaka,Kanie, Takashi,Kondo, Satoru

, p. 519 - 524 (2007/10/03)

Electrochemical oxidations of 1-tosyl-3-aryl-1,3-diazadihydroazulanones gave 6-tosyl-3-aryl-1,3-diazadihydroazulanones via migrations of the tosyl group. On the other hand, electrochemical reductions of the 1-tosyl- azulanones afforded 3-aryl-1,3-diazadih

-TYPE CYCLOADDITION REACTIONS OF N-ARYL-2,4,6-CYCLOHEPTATRIENE-1-IMINES AND 2,4,6-CYCLOHEPTATRIENE-1-THIONE WITH p-TOLUENESULFONYL ISOCYANATE: FORMATION OF 1,3-DIAZAAZULANONES

Ito, Kazuaki,Saito, Katsuhiro,Takeuchi, Shigeyuki,Takahashi, Kensuke

, p. 1415 - 1422 (2007/10/02)

Reactions of N-aryl-2,4,6-cycloheptatriene-1-imines and 2,4,6-cycloheptatriene-1-thione with p-toluenesulfonyl isocyanate gave -type cycloadducts in good yields.Eliminations of tosyl groups and dehydrogenations of the adducts afforded 1,3-diazaazulan

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