Welcome to LookChem.com Sign In|Join Free
  • or
2,6-Dibromo-4-(trifluoromethoxy)aniline is an organic compound characterized by the presence of two bromine atoms at the 2nd and 6th positions, and a trifluoromethoxy group at the 4th position attached to an aniline (amino) group. This unique molecular structure endows it with specific chemical properties that make it suitable for various applications, particularly in the synthesis of complex organic molecules.

88149-49-9

Post Buying Request

88149-49-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

88149-49-9 Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dibromo-4-(trifluoromethoxy)aniline is used as a key intermediate in the synthesis of novel pyridylpyrazole acid derivatives. These derivatives are of significant interest due to their potential applications in the development of new pharmaceutical compounds with improved therapeutic properties.
Used in Agricultural Industry:
2,6-Dibromo-4-(trifluoromethoxy)aniline is used as a chemical building block in the preparation of agricultural insecticides. Its unique structure allows for the creation of new insecticidal agents that can effectively control pests and protect crops, thereby contributing to increased agricultural productivity and food security.

Check Digit Verification of cas no

The CAS Registry Mumber 88149-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,4 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88149-49:
(7*8)+(6*8)+(5*1)+(4*4)+(3*9)+(2*4)+(1*9)=169
169 % 10 = 9
So 88149-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2F3NO/c8-4-1-3(14-7(10,11)12)2-5(9)6(4)13/h1-2H,13H2

88149-49-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • TCI America

  • (D3038)  2,6-Dibromo-4-(trifluoromethoxy)aniline  >98.0%(GC)

  • 88149-49-9

  • 5g

  • 490.00CNY

  • Detail

  • TCI America

  • (D3038)  2,6-Dibromo-4-(trifluoromethoxy)aniline  >98.0%(GC)

  • 88149-49-9

  • 25g

  • 1,390.00CNY

  • Detail

  • Alfa Aesar

  • (H55725)  2,6-Dibromo-4-(trifluoromethoxy)aniline, 97%   

  • 88149-49-9

  • 1g

  • 167.0CNY

  • Detail

  • Alfa Aesar

  • (H55725)  2,6-Dibromo-4-(trifluoromethoxy)aniline, 97%   

  • 88149-49-9

  • 5g

  • 960.0CNY

  • Detail

88149-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dibromo-4-(trifluoromethoxy)aniline

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-5-AminoTrifluoromethoxybenzene

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:88149-49-9 SDS

88149-49-9Upstream product

88149-49-9Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

-

Page/Page column 297-298, (2020/06/10)

In one aspect, compounds of Formula A, or a pharmaceutically acceptable salt thereof, are featured (Formula A) or a pharmaceutically acceptable salt thereof, wherein the variables shown in Formula A can be as defined anywhere herein.

Preparation method of 2,6-dibromo-4-trifluoromethoxyaniline

-

Paragraph 0012; 0022-0027, (2019/03/15)

The invention relates to a preparation method of 2,6-dibromo-4-trifluoromethoxyaniline, and belongs to the field of preparation of fine chemical engineering products. The preparation method of 2,6-dibromo-4-trifluoromethoxyaniline comprises the following

Preparation method of thifluzamide key intermediate, namely 2,6-dibromo-4-(trifluoromethoxy)aniline

-

Paragraph 0022-0033, (2017/08/29)

The invention discloses a preparation method of a thifluzamide key intermediate, namely 2,6-dibromo-4-(trifluoromethoxy)aniline. The method comprises the following operating steps: (1) adding water into a reaction bottle, dropwise adding concentrated sulf

Catalytic asymmetric pictet-spengler-type reaction for the synthesis of optically active indolo[3,4-cd][1]benzazepines

Cheng, Dao-Juan,Wu, Hai-Bian,Tian, Shi-Kai

supporting information; experimental part, p. 5636 - 5639 (2011/12/02)

A new strategy has been introduced to develop a catalytic asymmetric Pictet-Spengler-type reaction by replacing the aldehyde with an imine. A range of 4-(2-aminoaryl)indoles smoothly undergo the chiral phosphoric acid catalyzed asymmetric Pictet-Spengler-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 88149-49-9