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3484-33-1

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3484-33-1 Usage

Appearance

Yellow, crystalline solid This compound is a yellow-colored solid that forms crystals.

Usage

Reagent in chemical synthesis and research It is commonly used as a reagent in various chemical reactions and studies.

Derivative

Benzoic acid 2-(Methylamino)-5-nitrobenzoic acid is derived from benzoic acid.

Substituents

Methylamino group and nitro group These two functional groups are attached to the benzene ring in the compound.

Stability

Forms stable salts and complexes This compound is known for its ability to create stable salts and complexes, which is useful in various applications.

Applications

Pharmaceutical, agrochemical, and dye industries It has a wide range of applications in different industries, including the production of pharmaceuticals, agrochemicals, and dyes.

Biological activity

Potential antimicrobial and antitumor agent 2-(Methylamino)-5-nitrobenzoic acid has been investigated for its possible biological activities, such as fighting infections and inhibiting tumor growth.

Check Digit Verification of cas no

The CAS Registry Mumber 3484-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3484-33:
(6*3)+(5*4)+(4*8)+(3*4)+(2*3)+(1*3)=91
91 % 10 = 1
So 3484-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O4/c1-9-7-3-2-5(10(13)14)4-6(7)8(11)12/h2-4,9H,1H3,(H,11,12)

3484-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methylamino)-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Methylamino-5-nitro-benzoesaeure

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:3484-33-1 SDS

3484-33-1Relevant articles and documents

Alkylaminonitrobenzenes by Vicarious Nucleophilic Amination with 4-(Alkylamino)-1,2,4-triazoles

Katritzky, Alan R.,Laurenzo, Kathleen S.

, p. 3978 - 3982 (2007/10/02)

A series of 4-(alkylamino)-1,2,4-triazoles transfer the alkylamino group to the 4-position of nitrobenzene and various 3-substituted nitrobenzenes, with no detectable ortho substitution.By contrast 2-nitrothiophene reacts in the 3-position and 2-nitronaphthalene in the 1-position; 1-nitronaphthalene gives a mixture of products derived from dominant 2- with some 4-substitution.The orientations are discussed and rationalized.

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