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N-(benzhydrylideneamino)-N-methyl-aniline, also known as N,N'-dimethyl-N'-phenylbenzene-1,2-diamine, is an organic compound with the chemical formula C15H16N2. It is a derivative of aniline, featuring a benzhydryl group (a diphenylmethyl group) and a methyl group attached to the nitrogen atoms. N-(benzhydrylideneamino)-N-methyl-aniline is characterized by its aromatic structure and is used in various chemical syntheses, particularly in the production of dyes and pigments. It is also known for its potential applications in the pharmaceutical industry. The compound is typically synthesized through a condensation reaction involving aniline and formaldehyde in the presence of a catalyst. Due to its complex structure, it is important to handle this chemical with care, as it may have potential health and environmental impacts.

1665-83-4

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1665-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1665-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1665-83:
(6*1)+(5*6)+(4*6)+(3*5)+(2*8)+(1*3)=94
94 % 10 = 4
So 1665-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H18N2/c1-22(19-15-9-4-10-16-19)21-20(17-11-5-2-6-12-17)18-13-7-3-8-14-18/h2-16H,1H3

1665-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzhydrylideneamino)-N-methylaniline

1.2 Other means of identification

Product number -
Other names Benzophenon-N-methyl-N-phenylhydrazon

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:1665-83-4 SDS

1665-83-4Relevant academic research and scientific papers

Visible-Light-Induced Cycloaddition of α-Ketoacylsilanes with Imines: Facile Access to β-Lactams

Ye, Jian-Heng,Bellotti, Peter,Paulisch, Tiffany O.,Daniliuc, Constantin G.,Glorius, Frank

supporting information, p. 13671 - 13676 (2021/05/11)

We report the synthesis of β-lactams from α-ketoacylsilanes and imines, which proceeds via a formal [2+2] photochemical cycloaddition with in situ generation of siloxyketene. This mild and operationally simple reaction proceeds in an atom-economic fashion with broad substrate scope, including aldimines, ketimines, hydrazones, and fused nitrogen heterocycles, affording a variety of important β-lactams with satisfactory diastereoselectivities in most cases. This reaction also features good functional-group tolerance, facile scalability and product diversification. Experimental and computational studies suggest that α-ketoacylsilanes can serve as photochemical precursors by engaging in a 1,3 silicon shift to the distal carbonyl group.

Synthesis of β-lactams via cycloaddition of hydrazones with phenoxyketene

Sharma,Pandhi

, p. 2196 - 2200 (2007/10/02)

Phenoxyketene is capable of annelating the disubstituted hydrazones to afford stereoselectivity cis-monocyclic β-lactams with a 1-amino functionality. The ease of cycloaddition is governed by substitutents on the azomethine carbon as well as on the hydraz

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