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295376-29-3

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295376-29-3 Usage

Explanation

Different sources of media describe the Explanation of 295376-29-3 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. The compound is derived from benzene, a six-carbon ring with alternating single and double bonds, and has additional functional groups attached to it.
3. These functional groups are responsible for the compound's unique reactivity and properties.
4. The compound serves as a starting material or building block for the production of various drugs and chemicals used in agriculture.
5. The compound is utilized in research to create new organic molecules with potential applications in various fields.
6. The bromine and fluorine atoms in the structure contribute to the compound's unique chemical properties and reactivity, making it valuable in various chemical processes and applications.
7. Most organic compounds with molecular weights in this range are solids or liquids at room temperature, although the exact state depends on the compound's specific properties.
8. The compound is likely soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone due to its nonpolar nature.
9. The compound is expected to be stable under normal conditions, such as room temperature and pressure, without undergoing significant decomposition or reaction.
10. As with many organic compounds, 1-(benzyloxy)-3-bromo-2-fluorobenzene may pose health risks if not handled properly, such as being an irritant or toxic if ingested, inhaled, or absorbed through the skin. Proper safety precautions should be taken when working with this compound.

Structure

Substituted benzene compound

Functional groups

Benzyl ether, bromine atom, and fluorine atom

Applications

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Use in organic chemistry research

Building block for the production of other organic compounds

Unique reactivity

Presence of bromine and fluorine atoms

Physical state

Likely a solid or liquid at room temperature

Solubility

Soluble in organic solvents

Stability

Stable under normal conditions

Hazards

Potential irritant or toxic

Check Digit Verification of cas no

The CAS Registry Mumber 295376-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,5,3,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 295376-29:
(8*2)+(7*9)+(6*5)+(5*3)+(4*7)+(3*6)+(2*2)+(1*9)=183
183 % 10 = 3
So 295376-29-3 is a valid CAS Registry Number.

295376-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzyloxy)-3-bromo-2-fluorobenzene

1.2 Other means of identification

Product number -
Other names -

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:295376-29-3 SDS

295376-29-3Relevant articles and documents

Synthesis of novel 2H-spiro[1-benzofuran-3,4′-piperidin]ol scaffolds

Leflemme, Nicolas,Stoit, Axel R.,Borghese, Alfio

supporting information; experimental part, p. 2432 - 2435 (2012/06/01)

With the aim to enrich our 'privileged structure'-based library, novel 2H-spiro[1-benzofuran-3,4′-piperidin]ol scaffolds were prepared. The method involved a key intramolecular Heck cyclization which was successfully applied for three series of compounds.

NEW DISUBSTITUTED PHENYLPIPERIDINES/PIPERAZINES AS MODULATORS OF DOPAMINE NEUROTRANSMISSION

-

Page/Page column 64, (2008/06/13)

The present invention relates to compounds which have therapeutic effects against disorders in the central nervous system, and in particular new 4-(ortho, meta-disubstituted phenyl)-1-alkypiperidines and piperazines. (I) wherein R1, R2, R3 and Y are as de

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