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2-Nitro-3-aminobenzoic acid, an organic compound with the chemical formula C7H6N2O4, is a nitroaromatic compound featuring a nitro group and an amino group attached to a benzene ring, along with a carboxylic acid group. It is recognized for its potential as a pharmaceutical intermediate and as a building block in organic synthesis, making it an important compound in the field of organic chemistry.

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  • 116465-92-0 Structure
  • Basic information

    1. Product Name: 2-NITRO-3-AMINOBENZOIC ACID
    2. Synonyms: 3-AMINO-2-NITROBENZOIC ACID;2-NITRO-3-AMINOBENZOIC ACID;Benzoic acid, 3-aMino-2-nitro-
    3. CAS NO:116465-92-0
    4. Molecular Formula: C7H6N2O4
    5. Molecular Weight: 182.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116465-92-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 430.154°C at 760 mmHg
    3. Flash Point: 213.949°C
    4. Appearance: /
    5. Density: 1.569g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.682
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 2.35±0.10(Predicted)
    11. CAS DataBase Reference: 2-NITRO-3-AMINOBENZOIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-NITRO-3-AMINOBENZOIC ACID(116465-92-0)
    13. EPA Substance Registry System: 2-NITRO-3-AMINOBENZOIC ACID(116465-92-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 116465-92-0(Hazardous Substances Data)

116465-92-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Nitro-3-aminobenzoic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows it to undergo different chemical reactions, enabling the creation of derivatives with distinct properties and applications in the development of new medications.
Used in Dye Industry:
2-Nitro-3-aminobenzoic acid is also used in the synthesis of dyes. Its ability to form various derivatives through chemical reactions makes it a valuable component in the production of a wide range of dyes with different color characteristics and properties.
Used in Organic Synthesis:
As a building block in organic synthesis, 2-Nitro-3-aminobenzoic acid is utilized in the creation of complex organic compounds. Its versatile chemical properties make it an essential component in the synthesis of various organic compounds for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 116465-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,6 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116465-92:
(8*1)+(7*1)+(6*6)+(5*4)+(4*6)+(3*5)+(2*9)+(1*2)=130
130 % 10 = 0
So 116465-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O4/c8-5-3-1-2-4(7(10)11)6(5)9(12)13/h1-3H,8H2,(H,10,11)

116465-92-0 Well-known Company Product Price

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  • Aldrich

  • (JWP00063)  3-Amino-2-nitro-benzoic acid  AldrichCPR

  • 116465-92-0

  • JWP00063-1G

  • 5,151.51CNY

  • Detail

116465-92-0SDS

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 2-Nitro-3-aminobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-NITRO-3-AMINOBENZOIC 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:116465-92-0 SDS

116465-92-0Relevant articles and documents

A convenient copper-catalyzed direct animation of nitroarenes with 9-alkylhydroxylamines

Seko, Shinzo,Miyake, Kunihito,Kavvamura, Norio

, p. 1437 - 1444 (2007/10/03)

O-Alkylhydroxylamines, particularly O-methylhydroxylamine, aminate nitroarenes in the presence of a strong base and a copper catalyst to give aminonitroarenes in good yields, ortho- or para-Animation with respect to the nitro group takes place, and in some cases the ortho-aminated product is preferentially obtained. With 3-substituted nitrobenzenes where the substituent has a lone pair of electrons, preferential amination occurs at the 2-position to give the sterically most congested 3c-f, 14 and 22g.

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