Cas 90619-82-2,1,3-Benzenediamine, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-4,5,6-trifluoro-N,N'-dimethyl-N, N'-diphenyl-

90619-82-2

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Basic information

Product Name: 1,3-Benzenediamine, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-4,5,6-trifluoro-N,N'-dimethyl-N, N'-diphenyl-
Synonyms:
CAS NO:90619-82-2
Molecular Formula: C25H24F3N3O
Molecular Weight: 439.48
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: 1,3-Benzenediamine, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-4,5,6-trifluoro-N,N'-dimethyl-N, N'-diphenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-Benzenediamine, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-4,5,6-trifluoro-N,N'-dimethyl-N, N'-diphenyl-(90619-82-2)
EPA Substance Registry System: 1,3-Benzenediamine, 2-(4,5-dihydro-4,4-dimethyl-2-oxazolyl)-4,5,6-trifluoro-N,N'-dimethyl-N, N'-diphenyl-(90619-82-2)

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: 90619-82-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90619-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90619-82:
(7*9)+(6*0)+(5*6)+(4*1)+(3*9)+(2*8)+(1*2)=142
142 % 10 = 2
So 90619-82-2 is a valid CAS Registry Number.

90619-82-2Upstream product

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90619-82-2Relevant academic research and scientific papers

ORTHO-DISUBSTITUTED F-BENZENES - V. INTRAMOLECULAR HETEROATOM-FACILITATED ORTHO-SUBSTITUTION OF F-BENZENE DERIVATIVES WITH OXAZOLINYL AND OXAZINYL GROUPS.

Inukai,Takuma,Toritani,Sonoda,Kobayashi

, p. 225 - 231 (2007/10/02)

The oxazinyl and oxazolinyl substituents on an F-benzene ring facilitated the substitution of fluorine ortho to the heterocyclic functional groups by carbon and nitrogen nucleophiles. Alkylmagnesium halides and alkyllithium compounds were employed as the

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