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29103-60-4

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29103-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29103-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29103-60:
(7*2)+(6*9)+(5*1)+(4*0)+(3*3)+(2*6)+(1*0)=94
94 % 10 = 4
So 29103-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H22N2O/c1-18(25)23-21-13-8-14-22(15-21)24(16-19-9-4-2-5-10-19)17-20-11-6-3-7-12-20/h2-15H,16-17H2,1H3,(H,23,25)

29103-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[3-(dibenzylamino)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names EINECS 249-438-6

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:29103-60-4 SDS

29103-60-4Downstream Products

29103-60-4Relevant articles and documents

A Phosphine-Mediated Dearomative Skeletal Rearrangement of Dianiline Squaraine Dyes

Bacher, Emily P.,Koh, Kevin J.,Lepore, Antonio J.,Oliver, Allen G.,Wiest, Olaf,Ashfeld, Brandon L.

supporting information, p. 2853 - 2857 (2021/05/05)

A phosphorus(III)-mediated dearomatization of ortho-substituted dianiline squaraine dyes results in an unusual skeletal rearrangement to provide exotic, highly conjugated benzofuranone and oxindole scaffolds bearing a C3 side chain comprised of a linear conflagration of an enol, a phosphorus ylide, and 2,4-disubstituted aniline. Employing experimental and computational analysis, a mechanistic evaluation revealed a striking dependence on the acidity of the aniline ortho substituent. Notably, the rearrangement adducts underwent rapid and complete reversion to the parent squaraine in the presence of a Br?nsted acid.

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