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Methyl 4-[[(4-methoxyphenyl)methylene-]amino]benzoate is a complex organic chemical compound with the molecular formula C16H15NO4. It is a derivative of benzoic acid, featuring a methyl ester group, a 4-methoxyphenyl group, and an imine functional group. methyl 4-[[(4-methoxyphenyl)methylene-]amino]benzoate is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is characterized by its ability to form a Schiff base with aldehydes or ketones, which can be further utilized in various chemical reactions. The compound's properties, such as its solubility and stability, make it a valuable intermediate in the preparation of more complex molecules.

4112-08-7

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4112-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4112-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4112-08:
(6*4)+(5*1)+(4*1)+(3*2)+(2*0)+(1*8)=47
47 % 10 = 7
So 4112-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO3/c1-19-15-9-3-12(4-10-15)11-17-14-7-5-13(6-8-14)16(18)20-2/h3-11H,1-2H3/b17-11+

4112-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[(4-methoxyphenyl)methylideneamino]benzoate

1.2 Other means of identification

Product number -
Other names EINECS 223-896-7

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:4112-08-7 SDS

4112-08-7Relevant academic research and scientific papers

Visible-light-responsive multielectron redox catalysis of lacunary polyoxometalates induced by substrate coordination to their lacuna

Suzuki, Kosuke,Jeong, Jinu,Yamaguchi, Kazuya,Mizuno, Noritaka

supporting information, p. 144 - 148 (2015/02/19)

We describe herein the efficient visible-light-responsive polyoxometalate-based multielectron photoredox catalysis induced by in situ coordination of alcohols to the lacuna of TBA4H4[γ-SiW10O36] (I, TBA=tetra-n-butylammonium). The coordination of alcohols to the lacuna of I generated a new highest occupied molecular orbital as the electron donor level and enabled the visible-lightresponsive multielectron transfer from alcohols to I, which could be utilized for aerobic alcohol oxidation and onepot synthesis of N-arylimines starting from nitroarenes and primary alcohols.

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