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53304-12-4

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53304-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53304-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,0 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53304-12:
(7*5)+(6*3)+(5*3)+(4*0)+(3*4)+(2*1)+(1*2)=84
84 % 10 = 4
So 53304-12-4 is a valid CAS Registry Number.

53304-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-4-[(4-methylanilino)methylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names (4-Oxy-3-methoxy-benzal)-p-toluidin

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:53304-12-4 SDS

53304-12-4Relevant articles and documents

Chitosan: A highly efficient renewable and recoverable bio-polymer catalyst for the expeditious synthesis of α-amino nitriles and imines under mild conditions

Dekamin, Mohammad G.,Azimoshan, Mojtaba,Ramezani, Leila

supporting information, p. 811 - 820 (2013/04/10)

Commercial chitosan-without any post-modification with active Bronsted or Lewis acid centers-was found to be a highly efficient renewable and recoverable bio-polymer catalyst for the rapid and convenient synthesis of α-amino nitriles or imines from aromatic aldehydes and amines under mild reaction conditions at room temperature in high to quantitative yields. The α-amino nitrile derivatives were prepared through the Strecker reaction using trimethylsilyl cyanide (TMSCN) and catalyzed by chitosan as a heterogeneous bifunctional organocatalyst.

Synthesis, physicochemical characteristics and biological activity of ruthenium(III) complexes with bidentate (N, O) Schiff bases

Mehta, Bipin H.,Disale, Sameer D.

, p. 315 - 322 (2012/10/29)

The octahedral ruthenium(III) complexes have been prepared with bidentate Schiff bases derived from condensation of 2-amino-4-methylpyridine and 4-methylaniline with aromatic aldehydes. The obtained complexes were characterized on the basis of their eleme

Synthesis, characterization and thermal studies of Rh(III) complexes derived from bidentate schiff bases

Disale, Sameer,Pawanoji, Aniket,Mehta, Bipin

experimental part, p. 802 - 806 (2012/01/03)

The Schiff base ligands were derived from 2-hydroxy-3-methoxybenzaldehyde (HL1), 4-hydroxy-3-methoxybenzaldehyde (HL2), with p-toluidine and 3-hydroxybenzaldehyde with 4-hydroxybenzhydrazide (HL 3) and 3-hydroxy-2-naphthoi

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