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Benzoic acid, 4-chloro-2-[(4-methylphenyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32305-30-9

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32305-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32305-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32305-30:
(7*3)+(6*2)+(5*3)+(4*0)+(3*5)+(2*3)+(1*0)=69
69 % 10 = 9
So 32305-30-9 is a valid CAS Registry Number.

32305-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methylphenyl)amino]-5-chlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-chloro-2-p-toluidino-benzoic acid

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:32305-30-9 SDS

32305-30-9Relevant academic research and scientific papers

A rapid, chromatography-free route to substituted acridine-isoalloxazine conjugates under microwave irradiation

Johns, Stephen C.,Crouch, Laurie L.E.,Grieve, Stephen,Maloney, Holly L.,Peczkowski, Gary R.,Jones, Allison E.,Sharp, Duncan,Smith, Robert B.

supporting information, p. 3308 - 3311 (2014/06/09)

Microwave irradiation was applied to a sequence of condensation reactions from readily available 9-chloroacridines to provide a range of novel acridine-isoalloxazine conjugates. The combination of these two moieties, both of biological interest, was achieved by a chromatography-free route.

Fast synthesis of substituted N-phenylanthranilic acids using Ullmann condensation under microwave irradiation in dry media

Martin, Ana,Mesa, Miriam,Docampo, Maite L.,Gomez, Victoria,Pellon, Rolando F.

, p. 271 - 277 (2007/10/03)

Substituted N-phenylanthranilic acids using the Ullmann condensation under microwave irradiation in dry media were obtained in good yield and short reaction times. Copyright Taylor & Francis LLC.

Microwave-assisted synthesis of N-phenylanthranilic acids in water

Martin, Ana,Pellon, Rolando F.,Mesa, Miriam,Docampo, Maite L.,Gomez, Victoria

, p. 561 - 563 (2007/10/03)

N-Phenylanthranilic acid derivatives were synthesised using the Ullmann condensation of 2-chlorobenzoic acid with aniline derivatives under microwave irradiation in aqueous media. The method offers better yields in shorter reaction times compared to classical heating approaches using water as solvent.

Influence of the reaction conditions in the N-alkylation of acridone-2-Carboxylic acids

Marill,Pellon Comdom,Hernandez

, p. 2159 - 2167 (2007/10/03)

The synthesis and a study about the influence of the solvent in the alkylation reaction of 2-Carboxy-6-chloro-9(10H) acridone (3b) and 2-Carboxy-6-chloro-7-nitro-9(10H) acridone (3a) was done, obtaining the N-ethyl ester derivative of the alkylated produc

The Intercalation of 6-Chloro-substituted-9-amino>acridines with DNA

Kitchen, S. E.,Wang, Yueh-Hwa,Baumstark, A. L.,Wilson, W. D.,Boykin, D. W.

, p. 940 - 944 (2007/10/02)

A series of 6-chloro-2-substituted -9-amino>acridines has been prepared.The binding affinities and the unwinding angles for the acridine derivatives, relative to ethidium, were determined from viscometric titrations with ccs-DNA.

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