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Amino-F acid, also known as 4-amino-3-fluorobenzoic acid, is an organic compound with the chemical formula C7H6FNO2. It is a derivative of benzoic acid, featuring a fluorine atom at the 3-position and an amino group at the 4-position. amino-F acid is a white crystalline solid and is soluble in water and polar organic solvents. Amino-F acid has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. It can be used as an intermediate in the production of various compounds, such as fluorinated drugs and other fluorinated organic molecules, which may exhibit different properties compared to their non-fluorinated counterparts.

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  • 494-44-0 Structure
  • Basic information

    1. Product Name: amino-F acid
    2. Synonyms: 7-aminonaphthalene-2-sulphonic acid;amino-F acid;7-aminonaphthalene-2-sulfonic acid;2-Naphthylamine-7-sulfonic acid;7-Amino-2-naphthalenesulfonic acid;2-Amino-7-naphthalenesulfonic acid;7-azanylnaphthalene-2-sulfonic acid
    3. CAS NO:494-44-0
    4. Molecular Formula: C10H9NO3S
    5. Molecular Weight: 223.24836
    6. EINECS: 207-789-2
    7. Product Categories: N/A
    8. Mol File: 494-44-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.3588 (rough estimate)
    6. Refractive Index: 1.6500 (estimate)
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.16±0.40(Predicted)
    10. Water Solubility: 0.2g/L(20 oC)
    11. CAS DataBase Reference: amino-F acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: amino-F acid(494-44-0)
    13. EPA Substance Registry System: amino-F acid(494-44-0)
  • 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: 494-44-0(Hazardous Substances Data)

494-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494-44-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 494-44:
(5*4)+(4*9)+(3*4)+(2*4)+(1*4)=80
80 % 10 = 0
So 494-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3S/c11-9-3-1-7-2-4-10(15(12,13)14)6-8(7)5-9/h1-6H,11H2,(H,12,13,14)

494-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name amino-F acid

1.2 Other means of identification

Product number -
Other names 7-Amino-2-naphthalenesulfonic 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:494-44-0 SDS

494-44-0Relevant articles and documents

Reactive dye having both monochlorotriazinyl and vinylsulfone type reactive groups

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, (2008/06/13)

A novel reactive monoazo dye, capable of giving cellulose fiber materials a deep orange to scarlet color and superior in build-up and chlorine fastness properties, represented by a free acid of the formula, STR1 wherein R1 is hydrogen, methyl or ethyl; R2 is an alkyl having 1 to 4 carbons that is either unsubstituted or substituted with hydroxy, cyano, alkoxy, halogen, carboxy, alkoxycarbonyl or sulfonic acid; Z is hydrogen or sulfonic acid; A is phenylene and is either unsubstituted or substituted with 1 or 2 substituents selected from the group consisting of methyl, ethyl, methoxy, ethoxy, chlorine, bromine and sulfonic acid, or natphthylene that is either unsubstituted or substituted with sulfonic acid; X is --SO2 CH=CH2 or --SO2 CH2 CH2 Y in which Y is a group that is splittable by alkalis; and m is an integer of 1 to 3.

Fiber reactive monoazo compounds having two vinylsulfone type fiber reactive groups in the molecule

-

, (2008/06/13)

A monoazo compound of the following formula in a free acid form, STR1 wherein A1 and A2 are phenylene or naphthylene, Z1 and Z2 are --SO2 CH=CH2 or --SO2 CH2 CH2 Y in which Y is a splittable group, R1 and R2 are hydrogen or alkyl, and D is sulfophenyl or sulfonaphthyl, provided that --A1 --Z1 and --A2 --Z2 are different from each other when D is sulfophenyl and both R1 and R2 are hydrogen, which is useful for dyeing or printing fiber materials to give dyed products of high fastness properties with extremely high color depth.

Fiber-reactive disazo brown dye having vinylsulfone-type reactive group

-

, (2008/06/13)

A compound, or a salt thereof, represented by the following formula, STR1 wherein A is a substituted or unsubstituted phenylene or naphthylene group, B is STR2 in which R3 is a hydrogen atom or a lower alkyl, lower alkoxy, acylamino or ureido group, and R4 is a hydrogen atom or a lower alkyl or lower alkoxy group, R1 and R3 are independently a hydrogen atom or a substituted or unsubstituted lower alkyl group, X is a substituted or unsubstituted amino, lower alkoxy, substituted phenoxy or sulfo group, Y is --SO2 CH=CH2 or --SO2 CH2 CH2 Z, in which Z is a group capable of being split by the action of an alkali, and m is 2 or 3, which is useful for dyeing hydroxyl group- or amide group-containing fiber materials to give dyed products of a brown color having excellent fastness properties with good build-up property.

Process for monoacylating water-soluble organic amino compounds

-

, (2008/06/13)

A process for the monoacylation of water-soluble organic amino compounds with 2,4,6-trifluoro-s-triazine, which comprises introducing all reactants simultaneously and continuously in the amounts necessary for the required throughput into the reaction space and removing the resultant reaction products continuously therefrom.

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