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2-Amino-3,6-dimethylbenzoic acid is a chemical compound with the formula C9H11NO2, featuring a benzene ring with two methyl groups and an amino group attached to it. It is a derivative of benzoic acid and has potential antioxidant and antibacterial properties.
Used in Pharmaceutical Industry:
2-Amino-3,6-dimethylbenzoic acid is used as a building block for the synthesis of various drugs and pharmaceutical products. Its potential antioxidant and antibacterial properties make it a valuable ingredient in the development of new medications.
Used in Dye and Pigment Production:
2-Amino-3,6-dimethylbenzoic acid is used as a key component in the production of dyes, pigments, and organic synthesis, contributing to the color and stability of these products.
Used in Organic Synthesis:
2-Amino-3,6-dimethylbenzoic acid is utilized in organic synthesis for the creation of various chemical compounds, highlighting its versatility and importance in the field of chemistry.

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  • 15540-91-7 Structure
  • Basic information

    1. Product Name: 2-Amino-3,6-dimethylbenzoicacid
    2. Synonyms: 2-Amino-3,6-dimethylbenzoicacid;3,6-Dimethylanthanilic acid
    3. CAS NO:15540-91-7
    4. Molecular Formula: C9H11NO2
    5. Molecular Weight: 165.18914
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15540-91-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 319.8°Cat760mmHg
    3. Flash Point: 147.2°C
    4. Appearance: /
    5. Density: 1.207g/cm3
    6. Vapor Pressure: 0.000138mmHg at 25°C
    7. Refractive Index: 1.604
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Amino-3,6-dimethylbenzoicacid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Amino-3,6-dimethylbenzoicacid(15540-91-7)
    12. EPA Substance Registry System: 2-Amino-3,6-dimethylbenzoicacid(15540-91-7)
  • 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: 15540-91-7(Hazardous Substances Data)

15540-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15540-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,4 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15540-91:
(7*1)+(6*5)+(5*5)+(4*4)+(3*0)+(2*9)+(1*1)=97
97 % 10 = 7
So 15540-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-5-3-4-6(2)8(10)7(5)9(11)12/h3-4H,10H2,1-2H3,(H,11,12)

15540-91-7SDS

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 2-amino-3,6-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3,6-dimethyl-2-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:15540-91-7 SDS

15540-91-7Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS ANTIBIOTIC POTENTIATORS

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Paragraph 1159, (2016/07/05)

The invention relates to heterocyclic compounds and their use as antibiotics and/or as antibiotic potentiators. The compounds may act as colistin potentiators and SOS inhibitors.

TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES

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Page/Page column 983, (2013/11/18)

The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.

Electroorganic reactions. Part 55. Quinodimethane chemistry. Part 3. Transition metal complexes as inter- and intra-molecular redox catalysts for the electrosynthesis of poly(p-xylylene) (PPX) polymers and oligomers

Janssen,Utley,Carre?,Simon,Schirmer

, p. 1573 - 1584 (2007/10/03)

The role of metal complexes as redox mediators in the electrosynthesis of poly(p-xylylenes) (PPXs) has been explored, with a view to designing metal-containing precursors that can act both as mediators and starting materials for metal-containing polymers. A number of transition metal complexes [Cr(III), Ni(II) and Co(II)] are efficient redox catalysts for production of quinodimethanes, and hence PPXs. Following encouraging results from experiments using mediators based on anthranilic acid and salicylaldehyde ligands a macrocyclic compound was designed, and successfully prepared by a convergent route that incorporated both a 1,4-bis(chloromethylarene) function as a precursor to a quinodimethane and a Ni(II) salen unit as an intramolecular redox catalyst. The macrocycle was successfully reduced cathodically to yield a PPX polymer with bound Ni(II). Evidence is presented for the operation of intramolecular redox catalysis (homomediation).

Dicyclooctabiphenylene. Synthesis and Properties

Wilcox, Charles F.,Farley, Erik N.

, p. 7195 - 7200 (2007/10/02)

The synthesis and properties of the "antiaromatic" hydrocarbon dicyclooctabiphenylene (1) are described.The observed electronic and 1H NMR spectra of 1 agree well with previous predictions.The series of polycycles consisting o

Conformational Behaviour of Medium-sized Rings. Part 10. Dithiosalicylides and Trithiosalicylides

Guise, G. Bruce,Ollis, W. David,Peacock, Judith A.,Stephanatou, Julia Stephanidou,Stoddart, J. Fraser

, p. 1637 - 1648 (2007/10/02)

The trithiosalicylide derivatives (8)-(11) have been synthesised and shown by temperature-dependent 1H n.m.r. spectroscopy to exist in solution as ring inverting (35a)(35b) enantiomeric helical conformations with trans-thioester linkages.The free energies of activation for these conformational changes are ca. 10 kcal mol-1 higher than those for the similar process in the corresponding trisalicylides.In contrast with the trisalicylides, the trithiosalicylides can only ring invert between enantiomeric helical conformations via intermediates containing a cis-thioester linkage.The dithiosalicylide derivatives (3)-(7) have been synthesised; the temperature dependence of the 1H n.m.r. spectrum of di-o-thiothymotide (7) has been interpreted in terms of ring inversion (40a)(40b) between enantiomeric boat conformations.Comparison of the ΔG value of 24.6 kcal mol-1 for this conformational change with that of 17.7 kcal mol-1 previously obtained for di-o-thymotide (41) suggests that cis-thioester linkages are subject to more resonance stabilisation than are cis-ester linkages.

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