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α-tert-Butyl-N,α-diphenylbenzenemethanamine is a complex organic compound with the chemical formula C23H25N. It is a derivative of benzene, featuring a tert-butyl group (a carbon atom bonded to three methyl groups) attached to the alpha position, and two phenyl groups (each consisting of a benzene ring) attached to the nitrogen atom at the alpha position. α-tert-Butyl-N,α-diphenylbenzenemethanamine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a colorless to pale yellow solid and is typically used as an intermediate in the production of other chemicals. The compound's stability and reactivity can be influenced by factors such as temperature, light, and the presence of other reactive substances, making it important to handle and store it carefully in a controlled environment.

7714-61-6

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7714-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7714-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7714-61:
(6*7)+(5*7)+(4*1)+(3*4)+(2*6)+(1*1)=106
106 % 10 = 6
So 7714-61-6 is a valid CAS Registry Number.

7714-61-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethyl-N,1,1-triphenyl-propylamin

1.2 Other means of identification

Product number -
Other names (2,2-Dimethyl-1,1-diphenyl-propyl)-phenyl-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7714-61-6 SDS

7714-61-6Relevant academic research and scientific papers

Synthesis of N- and p-(Diphenylmethyl)anilines. ESR Study of their Photofragmentation

Siskos, Michael G.,Garas, Stylianos K.,Zarkadis, Antonios K.,Bokaris, Efthymios P.

, p. 2477 - 2482 (2007/10/02)

The reaction of N-substituted anilines 2 with diphenylmethyl halides 1 at room temperature in the presence of AlCl3 affords p-substituted derivatives 3 in good yields according to an electrophilic aromatic substitution.In contrast, aniline itself is only converted to the N-substituted compounds 4.A novel rearrangement from Ph3C-NHPh (4c) to p-(triphenylmethyl)aniline (5) is described.Unexpected photofragmentations of 4a, b are studied by using ESR and ENDOR spectroscopy; e.g., irradiation of 4b with quartz- or pyrex-filtered light leads to the formation of the radicals Ph2C-SiMe3 (7b) and Ph2C-NHPh (6) respectively, following selective cleavage of the C-N and C-Si bond.Key Words: Benzenamine derivatives, synthesis of / Rearrangement, Hofmann-Martius / Diphenylmethyl radicals / ESR measurements / ENDOR measurements

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