263397
3,5-Bis(trifluoromethyl)benzyl bromide
97%
Synonym(s):
1-(Bromomethyl)-3,5-bis(trifluoromethyl)benzene
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.445 (lit.)
density
1.675 g/mL at 25 °C (lit.)
functional group
bromo
fluoro
SMILES string
FC(F)(F)c1cc(CBr)cc(c1)C(F)(F)F
InChI
1S/C9H5BrF6/c10-4-5-1-6(8(11,12)13)3-7(2-5)9(14,15)16/h1-3H,4H2
InChI key
ATLQGZVLWOURFU-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
3,5-Bis(trifluoromethyl)benzyl bromide has been used:
- as derivatization reagent in detection of uracil in DNA by GC and negative chemical ionization mass spectrometry
- in enantioselective synthesis of non-peptidic neurokinin NK1 receptor antagonist, L-733,060
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
78.8 °F - closed cup
Flash Point(C)
26 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Analytical biochemistry, 219(2), 195-200 (1994-06-01)
A sensitive method using gas chromatography and negative chemical ionization mass spectrometry for the detection of uracil in DNA is described. Uracil DNA glycosylase is used to specifically cleave uracil from DNA. Once removed, uracil is derivatized with 3,5-bis(trifluoromethyl)benzyl bromide
Stereoselective synthesis of L-733,060.
Tetrahedron Letters, 44(5), 915-917 (2003)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service