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2-Amino-3-fluorobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 825-22-9 Structure
  • Basic information

    1. Product Name: 2-Amino-3-fluorobenzoic acid
    2. Synonyms: BUTTPARK 22\01-93;2-AMINO-3-FLUOROBENZENECARBOXYLIC ACID;2-AMINO-3-FLUOROBENZOIC ACID;3-FLUOROANTHRANILIC ACID;2-AMINO-3-FLUOROBENZOIC;Benzoic acid, 2-amino-3-fluoro-;3-Fluoroanthranilic acid, 2-Carboxy-6-fluoroaniline;Diaphonic acid
    3. CAS NO:825-22-9
    4. Molecular Formula: C7H6FNO2
    5. Molecular Weight: 155.13
    6. EINECS: 1308068-626-2
    7. Product Categories: Fluorin-contained Benzoic acid series;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Fluorine series
    8. Mol File: 825-22-9.mol
  • Chemical Properties

    1. Melting Point: 171-172°C
    2. Boiling Point: 294.4 °C at 760 mmHg
    3. Flash Point: 131.8 °C
    4. Appearance: white to light yellow crystal powder
    5. Density: 1.43 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Room temperature.
    8. Solubility: soluble in Methanol
    9. PKA: 4.60±0.10(Predicted)
    10. CAS DataBase Reference: 2-Amino-3-fluorobenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Amino-3-fluorobenzoic acid(825-22-9)
    12. EPA Substance Registry System: 2-Amino-3-fluorobenzoic acid(825-22-9)
  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 36/37/38-22
    3. Safety Statements: 26-36/37/39-24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 825-22-9(Hazardous Substances Data)

825-22-9 Usage

Chemical Properties

white to light yellow crystal powder

Check Digit Verification of cas no

The CAS Registry Mumber 825-22-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 825-22:
(5*8)+(4*2)+(3*5)+(2*2)+(1*2)=69
69 % 10 = 9
So 825-22-9 is a valid CAS Registry Number.

825-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-fluorobenzoic Acid

1.2 Other means of identification

Product number -
Other names 2-Amino-3-fluorobenzoic 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:825-22-9 SDS

825-22-9Relevant articles and documents

Weak, bidentate chelating group assisted cross-coupling of C(sp3)-H bonds in aliphatic acid derivatives with aryltrifluoroborates

Cai, Zhihua,Li, Shangda,Gao, Yuzhen,Fu, Lei,Li, Gang

supporting information, p. 12766 - 12769 (2018/11/23)

A protocol of Pd(ii)-catalyzed, weak bidentate directing group assisted β-C(sp3)-H activation/cross-coupling with organoboron reagents has been achieved, affording arylation of aliphatic acid derivatives that contain α-hydrogen atoms in moderate to good yields. The potential of this method for an asymmetric β-C(sp3)-H arylation via desymmetrization was also presented.

Substituents effects on activity of kynureninase from Homo sapiens and Pseudomonas fluorescens

Maitrani, Chandan,Phillips, Robert S.

, p. 4670 - 4677 (2013/07/26)

A series of substituted kynurenines (3-bromo-dl, 3-chloro-dl, 3-fluoro-dl, 3-methyl-dl, 5-bromo-l, 5-chloro-l, 3,5-dibromo-l and 5-bromo-3-chloro-dl) have been synthesized and tested for their substrate activity with human and Pseudomonas fluorescens kynureninase. All of the substituted kynurenines examined have substrate activity with both human as well as P. fluorescens kynureninase. For the human enzyme, 3- and 5-substituted kynurenines have k cat and kcat/Km values higher than l-kynurenine, but less than that of the physiological substrate, 3-hydroxykynurenine. However, 3,5-dibromo- and 5-bromo-3-chlorokynurenine have kcat and kcat/Km values close to that of 3-hydroxykynurenine with human kynureninase. The effects of the 3-halo substituents on the reactivity with human kynureninase may be due to electronic effects and/or halogen bonding. In contrast, for the bacterial enzyme, 3-methyl, 3-halo and 3,5-dihalokynurenines are much poorer substrates, while 3-fluoro, 5-bromo, and 5-chlorokynurenine have kcat and kcat/K m values comparable to that of its physiological substrate, l-kynurenine. Thus, 5-bromo and 5-chloro-l-kynurenine are good substrates for both human as well as bacterial enzyme, indicating that both enzymes have space for substituents in the active site near C-5. The increased activity of the 5-halokynurenines may be due to van der Waals contacts or hydrophobic effects. These results may be useful in the design of potent and/or selective inhibitors of human and bacterial kynureninase.

Synthesis of insecticidal fluorinated anthranilic diamides

Clark, David A.,Lahm, George P.,Smith, Ben K.,Barry, James D.,Clagg, Don G.

, p. 3163 - 3170 (2008/09/20)

A series of highly active fluorinated anthranilic diamide insecticides have been prepared and their biological activity assessed on two aphid species in the search for systemically active compounds that control Hemiptera. In addition, we have demonstrated a new synthesis of N-aryl 3-fluoropyrazoles.

Condensed pyrazole derivatives, process for producing the same and use thereof

-

, (2008/06/13)

Novel pharmaceutical compositions for inhibiting Th2-selective immune response and pharmaceutical compositions for inhibiting cyclooxygenase comprising condensed pyrazole derivatives represented by the general formula (I): or salts thereof.

Antimicrobial activity of fluorinated 1,2-benzisothiazol-3(2H)-ones and 2,2'-dithiobis(benzamides)

Carmellino,Pagani,Pregnolato,Terreni,Pastoni

, p. 743 - 751 (2007/10/02)

Fluoro and trifluoromethyl derivatives of 1,2-benzisothiazol-3(2H)-ones and the 2,2'-dithiobis(benzamides) have been prepared and their antifungal and antibacterial activity evaluated. Several compounds were found highly active against fungi and Gram-positive microorganisms and a few derivatives displayed some activity against Gram-negative strains. Structure-activity relationships are proposed.

Process for the preparation of 3- and/or 5-substituted anthranilic acids

-

, (2008/06/13)

Anthranilic acids substituted in the 3- and/or 5-position are valuable intermediates for the production of agricultural chemicals. These substituted anthranilic acids can be obtained in good yield without undesirable isomeric byproducts by the oxidative r

Synthetic Entries to 6-Fluoro-7-substituted Indole Derivatives

McKittrick, Brian,Failli, Amedeo,Steffan, Robert J.,Soll, Richard M.,Hughes, Philip,et al.

, p. 2151 - 2163 (2007/10/02)

Three practical synthetic entries of functionalized 6-fluoro-7-substituted indole derivatives were developed in connection with the preparation of 7-fluoro-8-substituted-1,3,4,9-tetrahydropyranoindole-1-acetic acid derivatives 11.The first route, w

Certain 1,3-dihydro-1-[heterocyclic)imino]-furo-[3,4-b]quinoline 9-ol compounds having analgesic and anti-inflammatory activity

-

, (2008/06/13)

A 4-hydroxy-3-quinoline-carboxamides of the formula STR1 wherein X is in the 5,6,7 or 8-position and is selected from the group consisting of hydrogen, halogen, alkyl of 1 to 5 carbon atoms, alkoxy of 1 to 4 carbon atoms, --CH3, --OCF3/su

AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF 3-FLUOROANTHRANILIC ACID

Milner, David J.

, p. 485 - 490 (2007/10/02)

3-Ffluoroanthranilic acid is derived in four steps from 3-nitrophthalic acid in 53percent overall yield.

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