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17299-95-5

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17299-95-5 Usage

General Description

1,5-dibromo-2,3,4-trifluorobenzene is a fluoride chemical compound distinct for its composition and combination of Bromine and Fluorine groups attached to a benzene ring. It expresses an aromatic nature due to the presence of stable benzene rings. The chemical formula is C6Br2F3. This chemical compound is used extensively in research and chemical industries due to its unique reactivity and stability, which makes it suitable for creating a multitude of different complex chemicals. Its physical, chemical, and toxicological properties are often used by researchers and chemists to push the boundaries of their work. It is a key intermediate in organic synthesis and may be used for the production of pharmaceuticals, agrochemicals, dyestuffs, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 17299-95-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 17299-95:
(7*1)+(6*7)+(5*2)+(4*9)+(3*9)+(2*9)+(1*5)=145
145 % 10 = 5
So 17299-95-5 is a valid CAS Registry Number.

17299-95-5SDS

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 1,5-dibromo-2,3,4-trifluorobenzene

1.2 Other means of identification

Product number -
Other names 4,5,6-Trifluor-1,3-dibrombenzol

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:17299-95-5 SDS

17299-95-5Relevant articles and documents

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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