Cas 94532-09-9,Benzenamine, 4-methyl-N-[2,2,2-trifluoro-1-[5-methyl-2-(1-pyrrolidinyl)phenyl]ethylidene ]-

94532-09-9

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Basic information

Product Name: Benzenamine, 4-methyl-N-[2,2,2-trifluoro-1-[5-methyl-2-(1-pyrrolidinyl)phenyl]ethylidene ]-
Synonyms:
CAS NO:94532-09-9
Molecular Formula: C20H21F3N2
Molecular Weight: 346.395
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: Benzenamine, 4-methyl-N-[2,2,2-trifluoro-1-[5-methyl-2-(1-pyrrolidinyl)phenyl]ethylidene ]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenamine, 4-methyl-N-[2,2,2-trifluoro-1-[5-methyl-2-(1-pyrrolidinyl)phenyl]ethylidene ]-(94532-09-9)
EPA Substance Registry System: Benzenamine, 4-methyl-N-[2,2,2-trifluoro-1-[5-methyl-2-(1-pyrrolidinyl)phenyl]ethylidene ]-(94532-09-9)

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: 94532-09-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94532-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94532-09:
(7*9)+(6*4)+(5*5)+(4*3)+(3*2)+(2*0)+(1*9)=139
139 % 10 = 9
So 94532-09-9 is a valid CAS Registry Number.

94532-09-9Upstream product

94532-09-9Downstream Products

94532-11-3 1,2,3,3a,4,5-hexahydro-7-methyl-4-(4-methylphenyl)-5-trifluoromethylpyrrolo<1,2-a>quinazoline

94532-09-9Relevant academic research and scientific papers

NOVEL APPLICATIONS OF THE "t-AMINO EFFECT" IN HETEROCYCLIC CHEMISTRY. SYNTHESIS OF A PYRROLOQUINAZOLINE AND 5H-PYRROLOBENZOTHIAZINES

Verboom, W.,Hamzink, M. R. J.,Reinhoudt, D. N.,Visser, R.

, p. 4309 - 4312 (1984)

1-(1-Pyrrolidinyl)benzenes substituted with an imino- or an in situ generated thiocarbonyl group in the 2-position rearrange upon heating to quinazoline and benzothiazine derivatives, respectively.

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