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  • 115467-07-7 Structure
  • Basic information

    1. Product Name: 3,5-Difluoro-4-(trifluoromethoxy)bromobenzene
    2. Synonyms: 3,5-Difluoro-4-(trifluoromethoxy)bromobenzene;4-BroMo-2,6-difluoro(trifluoroMethoxy)benzene;5-Bromo-1,3-difluoro-2-(trifluoromethoxy)benzene;2,6-Difluoro-4-bromotrifluoromethoxybenzene;4-Bromo-2,6-fluorotrifluoromethoxybenzene
    3. CAS NO:115467-07-7
    4. Molecular Formula: C7H2BrF5O
    5. Molecular Weight: 276.986196
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115467-07-7.mol
    9. Article Data: 1
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 175.315oC at 760 mmHg
    3. Flash Point: 72.901oC
    4. Appearance: /
    5. Density: 1.794g/cm3
    6. Vapor Pressure: 1.55mmHg at 25°C
    7. Refractive Index: 1.4330 to 1.4370
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,5-Difluoro-4-(trifluoromethoxy)bromobenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,5-Difluoro-4-(trifluoromethoxy)bromobenzene(115467-07-7)
    12. EPA Substance Registry System: 3,5-Difluoro-4-(trifluoromethoxy)bromobenzene(115467-07-7)
  • 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: 115467-07-7(Hazardous Substances Data)

115467-07-7 Usage

Chemical Properties

Colorless transparent liquid

Check Digit Verification of cas no

The CAS Registry Mumber 115467-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115467-07:
(8*1)+(7*1)+(6*5)+(5*4)+(4*6)+(3*7)+(2*0)+(1*7)=117
117 % 10 = 7
So 115467-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H2BrF5O/c8-3-1-4(9)6(5(10)2-3)14-7(11,12)13/h1-2H

115467-07-7 Well-known Company Product Price

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  • TCI America

  • (B5057)  5-Bromo-1,3-difluoro-2-(trifluoromethoxy)benzene  >98.0%(GC)

  • 115467-07-7

  • 1g

  • 790.00CNY

  • Detail
  • TCI America

  • (B5057)  5-Bromo-1,3-difluoro-2-(trifluoromethoxy)benzene  >98.0%(GC)

  • 115467-07-7

  • 5g

  • 2,360.00CNY

  • Detail

115467-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-1,3-difluoro-2-(trifluoromethoxy)benzene

1.2 Other means of identification

Product number -
Other names 3,5-DIFLUORO-4-(TRIFLUOROMETHOXY)BROMOBENZENE

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:115467-07-7 SDS

115467-07-7Upstream product

115467-07-7Relevant articles and documents

A 4 - bromo - 2, 6 - two fluorine three fluorine methoxybenzene preparation method

-

, (2018/07/06)

The invention relates to the field of organic synthesis, particularly a preparation method of 4-bromo-2, 6-difluorotrifluoromethoxybenzene. The preparation method of 4-bromo-2, 6-difluorotrifluoromethoxybenzene provided by the invention comprises the following steps: (1) esterification reaction: reacting 4-bromo-2, 6-difluorophenol with an esterification reagent in the presence of an alkali in a reaction solvent to generate 4-bromo-2, 6-difluoro-difluorobromomethoxybenzene or 4-bromo-2, 6-difluoro-difluorochloromethoxybenzene; and (2) fluoridation reaction: reacting the product obtained in the step (1) with a fluoridation reagent under the action of a catalyst to generate 4-bromo-2, 6-difluorotrifluoromethoxybenzene. The preparation method of 4-bromo-2, 6-difluorotrifluoromethoxybenzene, provided by the invention, is simple in process and mild in reaction condition, can be carried out at a normal pressure, and is suitable for industrial production.

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