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Home > Encyclopedia > 3,5-Bis(trifluoromethyl)benzyl bromide

3,5-Bis(trifluoromethyl)benzyl bromide

3,5-Bis(trifluoromethyl)benzyl bromide structure

3,5-Bis(trifluoromethyl)benzyl bromide 

structure
  • CAS No:

    32247-96-4

  • Formula:

    C9H5BrF6

  • Chemical Name:

    3,5-Bis(trifluoromethyl)benzyl bromide

  • Synonyms:

    Benzene,1-(bromomethyl)-3,5-bis(trifluoromethyl)-;Mesitylene,α′′-bromo-α,α,α,α′,α′,α′-hexafluoro-;1-(Bromomethyl)-3,5-bis(trifluoromethyl)benzene;3,5-Bis(trifluoromethyl)benzyl bromide;3,5-Di(trifluoromethyl)benzyl bromide;1-Bromomethyl-3,5-ditrifluoromethylbenzene;3,5-(Trifluoromethyl)benzyl bromide;1,3-Ditrifluoromethyl-5-bromobenzene

  • Categories:

    Organic Chemistry  >  Hydrocarbons and Derivatives

Description

light yellow liquid

3,5-Bis(trifluoromethyl)benzyl bromide Basic Attributes

307.03

307.03

656506

250-971-1

DTXSID10186001

2903999090

Characteristics

0

4.2

Clear colorless to yellow-brown Liquid

1.7±0.1 g/cm3

28-30ºC

136-140°C14mm

79 °F

1.438

Flammables area

Safety Information

8

UN 2920 8/PG 2

3

10-34

26-36/37/39-45-25-16

C,F

Corrosive/Lachrymatory

P280-P305 + P351 + P338-P310

H226-H314

|Danger|H226 (92.41%): Flammable liquid and vapor [Warning Flammable liquids]|P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, and P501|Aggregated GHS information provided by 79 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

3,5-bis(trifluoromethyl)benzyl bromide

3,5-Bis(trifluoromethyl)benzyl bromide Use and Manufacturing

Preparation of 3, 5-bis (trifluoromethyl)-benzyl bromide; In a 4-neck flask with capacity 1000 ml equipped with mechanical agitator, thermometer, bubble condenser and 100 ml loading funnel, 262.2 g of the product of (ii) at 92. 8percent (0. 988 moles), 550, 2 g HBr 48percent (3.2645 moles) are loaded; this is heated at 50°C so as to melt the alcohol, then one starts to dose 113 g of concentrated His04 (1.153 moles). Pouring is accomplished in 30 minutes, noting an increase of the internal temperature. This is heated to 100-105°C and left to react for 8 hours. The reaction is completed by reflux heating for per 1.5 hours. the mixture is left to settle and the phases are separated; the solvents are removed from the organic phase and the product in the title is obtained with a yield of 99.1 percent.

Computed Properties

Molecular Weight:307.03
XLogP3:4.2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:305.94788
Monoisotopic Mass:305.94788
Heavy Atom Count:16
Complexity:211
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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