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5-BROMO-4-FLUORO-2-METHYLANILINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 627871-16-3 Structure
  • Basic information

    1. Product Name: 5-BROMO-4-FLUORO-2-METHYLANILINE
    2. Synonyms: 2-Amino-4-bromo-5-fluorotoluene, 5-Bromo-4-fluoro-o-toluidine;BenzenaMine,5-broMo-4-fluoro-2-Methyl-;2-AMino-4-broMo-5-fluorotoluene[5-BroMo-4-fluoro-2-Methylaniline]
    3. CAS NO:627871-16-3
    4. Molecular Formula: C7H7BrFN
    5. Molecular Weight: 204.05
    6. EINECS: N/A
    7. Product Categories: Amines;C7;Nitrogen Compounds;Aryl Fluorinated Building Blocks;Building Blocks;C7-C8;Chemical Synthesis;Fluorinated Building Blocks;Nitrogen Compounds;Organic Building Blocks;Organic Fluorinated Building Blocks;Other Fluorinated Organic Building Blocks
    8. Mol File: 627871-16-3.mol
  • Chemical Properties

    1. Melting Point: 86-90 °C(lit.)
    2. Boiling Point: 266.3°C at 760 mmHg
    3. Flash Point: 114.9°C
    4. Appearance: /Solid
    5. Density: 1.589g/cm3
    6. Vapor Pressure: 0.00869mmHg at 25°C
    7. Refractive Index: 1.584
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 3.44±0.10(Predicted)
    11. CAS DataBase Reference: 5-BROMO-4-FLUORO-2-METHYLANILINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-BROMO-4-FLUORO-2-METHYLANILINE(627871-16-3)
    13. EPA Substance Registry System: 5-BROMO-4-FLUORO-2-METHYLANILINE(627871-16-3)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 627871-16-3(Hazardous Substances Data)

627871-16-3 Usage

Chemical Properties

light brown solid

Check Digit Verification of cas no

The CAS Registry Mumber 627871-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,8,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 627871-16:
(8*6)+(7*2)+(6*7)+(5*8)+(4*7)+(3*1)+(2*1)+(1*6)=183
183 % 10 = 3
So 627871-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrFN/c1-4-2-6(9)5(8)3-7(4)10/h2-3H,10H2,1H3

627871-16-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H62480)  5-Bromo-4-fluoro-2-methylaniline, 96%   

  • 627871-16-3

  • 1g

  • 376.0CNY

  • Detail
  • Alfa Aesar

  • (H62480)  5-Bromo-4-fluoro-2-methylaniline, 96%   

  • 627871-16-3

  • 5g

  • 1518.0CNY

  • Detail

627871-16-3SDS

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 5-Bromo-4-fluoro-2-methylaniline

1.2 Other means of identification

Product number -
Other names 5-BROMO-4-FLUORO-2-METHYLANILINE

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:627871-16-3 SDS

627871-16-3Relevant articles and documents

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

-

, (2016/05/02)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

Pinacol as a new green reducing agent: Molybdenum-catalyzed chemoselective reduction of sulfoxides and nitroaromatics

Garcia, Nuria,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Rubio, Ruben,Pedrosa, Maria R.,Arnaiz, Francisco J.,Sanz, Roberto

supporting information; experimental part, p. 321 - 327 (2012/04/11)

Pinacol is disclosed as a new chemoselective and environmentally benign reducing agent for sulfoxides and nitroaromatics assisted by readily available dichlorodioxomolybdenum(VI) complexes as catalysts. A wide range of substrates including those bearing challenging functional groups has been efficiently and selectively reduced with acetone and water being the only by-products of these reactions. Copyright

Design and synthesis of 3,4-dihydro-1H-[1]-benzothieno[2,3-c]pyran and 3,4-dihydro-1H-pyrano[3,4-b]benzofuran derivatives as non-nucleoside inhibitors of HCV NS5B RNA dependent RNA polymerase

Gopalsamy, Ariamala,Aplasca, Alexis,Ciszewski, Gregory,Park, Kaapjoo,Ellingboe, John W.,Orlowski, Mark,Feld, Boris,Howe, Anita Y.M.

, p. 457 - 460 (2007/10/03)

A novel class of HCV NS5B RNA dependent RNA polymerase inhibitors containing 3,4-dihydro-1H-[1]-benzothieno[2,3-c]pyran and 3,4-dihydro-1H- pyrano[3,4-b]benzofuran scaffolds were designed and synthesized. Optimization of the alkyl substituent in the pyran ring showed preference for an n-propyl group, while 5,8-disubstitution pattern is preferred for the aromatic region. Analog 19 displayed potent activity with an IC50 of 50 nM against HCV NS5B enzyme and was selective over a panel of polymerases.

Discovery of pyrano[3,4-b]indoles as potent and selective HCV NS5B polymerase inhibitors

Gopalsamy, Ariamala,Lim, Kitae,Ciszewski, Gregory,Park, Kaapjoo,Ellingboe, John W.,Bloom, Jonathan,Insaf, Shabana,Upeslacis, Janis,Mansour, Tarek S.,Krishnamurthy, Girija,Damarla, Murthy,Pyatski, Yelena,Ho, Douglas,Howe, Anita Y. M.,Orlowski, Mark,Feld, Boris,O'Connell, John

, p. 6603 - 6608 (2007/10/03)

A novel series of HCV NS5B RNA-dependent RNA polymerase inhibitors containing a pyrano-[3,4-b]indole scaffold is described leading to the discovery of compound 16, a highly potent and selective inhibitor that is active in the replicon system.

R-ENANTIOMERS OF PYRANOINDOLE DERIVATIVES AGAINST HEPATITIS C

-

Page 32, (2008/06/13)

The invention is directed to a compound and a pharmaceutical composition of the formula: Wherein substitutions at R1, R2, R3 - R12, and Y are set forth in the specification.

METHOD FOR THE USE OF PYRANOINDOLE DERIVATIVES TO TREAT INFECTION WITH HEPATITIS C VIRUS

-

Page 65, (2008/06/13)

The invention is directed to methods of treating, preventing, or inhibiting a Hepatitis C viral infection in a mammal comprising containing the mammal with an effective amount of a compound of the formula: Wherein substitutions at R1, R2, R3-R12, and Y are set forth in the specification.

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