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Benzamide, 4-methyl-N-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15563-78-7

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15563-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15563-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15563-78:
(7*1)+(6*5)+(5*5)+(4*6)+(3*3)+(2*7)+(1*8)=117
117 % 10 = 7
So 15563-78-7 is a valid CAS Registry Number.

15563-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzylidene-4-methylbenzamide

1.2 Other means of identification

Product number -
Other names 4-Methyl-N-(phenylmethylen)benzamid

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:15563-78-7 SDS

15563-78-7Relevant academic research and scientific papers

A convenient one-pot approach to Paclitaxel (Taxol) side chain via 1,3-dipolar cycloaddition of carbonyl ylides and N-benzoylbenzyl imines

Sheng, Jiajun,Chang, Huan,Qian, Yu,Ma, Mingliang,Hu, Wenhao

supporting information, p. 2141 - 2144 (2018/05/05)

An efficient cascade approach to α-hydroxy-β-amino acid derivatives is reported, which goes through a 1,3-dipolar cycloaddition of carbonyl ylides and N-benzoylbenzyl imines and followed by hydrolysis under acidic conditions. This is the first example of using N-benzoylbenzyl imine as dipolarophile for 1,3-dipolar cycloaddition with carbonyl ylide, which provides a direct and convenient access for the one-pot synthesis of paclitaxel side chain and its derivatives.

Modular synthesis of tetrasubstituted imidazoles and trisubstituted oxazoles by aldimine cross-coupling

Kison, Coralie,Opatz, Till

body text, p. 843 - 845 (2009/06/28)

A study was conducted to demonstrate the synthesis of tetrasubstituted imidazoles and trisubstituted oxazoles by aldimine cross-coupling reaction. The method involved 1,2-addition of easily available deprotonated N-monosubstituted α-aminotitriles to aldim

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