Cas 397-10-4,Benzenamine, N,N-dibutyl-3-(trifluoromethyl)-

397-10-4

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Basic information

Product Name: Benzenamine, N,N-dibutyl-3-(trifluoromethyl)-
Synonyms:
CAS NO:397-10-4
Molecular Formula: C15H22F3N
Molecular Weight: 273.342
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, N,N-dibutyl-3-(trifluoromethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenamine, N,N-dibutyl-3-(trifluoromethyl)-(397-10-4)
EPA Substance Registry System: Benzenamine, N,N-dibutyl-3-(trifluoromethyl)-(397-10-4)

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: 397-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 397-10-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 397-10:
(5*3)+(4*9)+(3*7)+(2*1)+(1*0)=74
74 % 10 = 4
So 397-10-4 is a valid CAS Registry Number.

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397-10-4Relevant academic research and scientific papers

Umpolung amination: Nickel-catalyzed coupling reactions of N,N-dialkyl-N-chloroamines with diorganozinc reagents

Barker, Timothy J.,Jarvo, Elizabeth R.

supporting information; experimental part, p. 15598 - 15599 (2010/01/29)

(Chemical Equation Presented) N,N-Dialkyl-N-chloroamines are an effective source of electrophilic nitrogen for nickel-catalyzed coupling with diarylzinc reagents. A variety of N-chloroamines as well as organozinc reagents react smoothly under the reaction conditions. A one-pot procedure that circumvents the need to isolate the N-chloroamines is described.

First palladium-catalyzed aminations of aryl chlorides

Beller, Matthias,Riermeier, Thomas H.,Reisinger, Claus-Peter,Herrmann, Wolfgang A.

, p. 2073 - 2074 (2007/10/03)

The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tert-butoxide as base. Turn over numbers up to 900 and y

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