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1,2-DIBROMO-3,4,5-TRIFLUOROBENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17299-94-4

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17299-94-4 Usage

Physical state

Colorless liquid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Building block in the synthesis of pharmaceuticals
b. Building block in the synthesis of agrochemicals
c. Intermediate in the production of dyes
d. Intermediate in the production of pigments
e. Intermediate in the production of other specialty chemicals

Chemical classification

Halogenated aromatic compound

Safety precautions

Handle with care due to toxic and potentially harmful properties

Check Digit Verification of cas no

The CAS Registry Mumber 17299-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,9 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17299-94:
(7*1)+(6*7)+(5*2)+(4*9)+(3*9)+(2*9)+(1*4)=144
144 % 10 = 4
So 17299-94-4 is a valid CAS Registry Number.

17299-94-4SDS

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 1,2-DIBROMO-3,4,5-TRIFLUOROBENZENE

1.2 Other means of identification

Product number -
Other names Benzene,1,2-dibromo-3,4,5-trifluoro

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:17299-94-4 SDS

17299-94-4Relevant academic research and scientific papers

Organometallic control over the regiospecificity of functionalization reactions: 1,2,3-Trifluorobenzene and bromo derivatives thereof as substrates

Heiss, Christophe,Schlosser, Manfred

, p. 447 - 451 (2007/10/03)

In a case study, 1,2,3-trifluorobenzene was functionalized at each of the two vacant positions (producing the benzoic acids 1 and 2) and, in addition, bromine was introduced into all available positions (producing the benzoic acids 3-5). The required regioflexibility was achieved by applying novel organometallic recipes such as deprotonation-triggered halogen migrations and site-discriminating competitive halogen-metal permutations. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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