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367-67-9

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367-67-9 Usage

Chemical Properties

yellow crystals

Uses

2-Bromo-5-nitrobenzotrifluoride may be used in the preparation of:new unsymmetrical diamine monomer containing both the benzimidazole ring and trifluoromethyl group, 6,4′-diamino-2′-trifluoromethyl-2-phenylbenzimidazole2,5-bis[(4-nitro-2-trifluoromethylphenoxy)-phenyl]diphenylphosphine oxide (BNTFDPO)

Check Digit Verification of cas no

The CAS Registry Mumber 367-67-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 367-67:
(5*3)+(4*6)+(3*7)+(2*6)+(1*7)=79
79 % 10 = 9
So 367-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrF3NO2/c8-5-1-4(7(9,10)11)2-6(3-5)12(13)14/h1-3H

367-67-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (A11416)  2-Bromo-5-nitrobenzotrifluoride, 97%   

  • 367-67-9

  • 5g

  • 368.0CNY

  • Detail
  • Alfa Aesar

  • (A11416)  2-Bromo-5-nitrobenzotrifluoride, 97%   

  • 367-67-9

  • 25g

  • 1141.0CNY

  • Detail
  • Aldrich

  • (365769)  2-Bromo-5-nitrobenzotrifluoride  97%

  • 367-67-9

  • 365769-5G

  • 332.75CNY

  • Detail
  • Aldrich

  • (365769)  2-Bromo-5-nitrobenzotrifluoride  97%

  • 367-67-9

  • 365769-25G

  • 1,347.84CNY

  • Detail

367-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-5-nitrobenzotrifluoride

1.2 Other means of identification

Product number -
Other names 2-BroMo-5-nitro trifluoroMethyl

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:367-67-9 SDS

367-67-9Relevant articles and documents

Fluorine-containing aromatic diamine compound and preparation method thereof, and fluorine-containing polyimide compound and preparation method thereof

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Paragraph 0146; 0151; 0152, (2021/01/29)

The invention provides a fluorine-containing aromatic diamine compound and a preparation method thereof, and a fluorine-containing polyimide compound and a preparation method thereof. The fluorine-containing aromatic diamine compound has a structural general formula shown in the specification. The preparation method of the fluorine-containing aromatic diamine compound comprises the following stepsof: mixing materials including a compound A and a compound B, carrying out a first reaction to obtain a compound C, and carrying out a hydrogenation reaction on the compound C to obtain the fluorine-containing aromatic diamine compound. Raw materials of the fluorine-containing polyimide compound comprise the fluorine-containing aromatic diamine compound. The preparation method of the fluorine-containing polyimide compound comprises the following steps of: mixing materials including the fluorine-containing aromatic diamine compound and a dianhydride compound to obtain a mixture, and then carrying out a sixth reaction to obtain a precursor; and carrying out dehydration cyclization reaction on the pre-polymer, and carrying out post-treatment to obtain the fluorine-containing polyimide compound. The polyimide compound prepared from the fluorine-containing aromatic diamine compound provided by the invention is good in solubility, relatively high in transmittance and good in mechanical property.

Synthesis method of 2-bromo-5-fluorobenzotrifluoride

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Paragraph 0020-0021, (2017/07/22)

The invention relates to a synthesis method of 2-bromo-5-fluorobenzotrifluoride, belonging to the field of chemical synthesis. The method uses orthotrifluoromethyl aniline as the initial raw material, and comprises the following steps: (1) Sandmeyer bromination reaction; (2) nitration reaction; (3) catalytic hydrogenation reduction reaction; and (4) diazotization fluorination reaction. According to the method, the orthotrifluoromethyl aniline used as the raw material is subjected to Sandmeyer reaction bromination, nitration, hydrogenation reduction and diazotization fluorination to finally synthesize the 2-bromo-5-fluorobenzotrifluoride. The 2-bromo-5-fluorobenzotrifluoride product has the advantages of high purity (up to 99.0% or above), fewer impurity varieties and stable quality and properties.

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