Skip to Content
MilliporeSigma
All Photos(3)

Documents

263389

Sigma-Aldrich

3,5-Bis(trifluoromethyl)benzylamine

technical grade, 80%

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
(CF3)2C6H3CH2NH2
CAS Number:
85068-29-7
Molecular Weight:
243.15
Beilstein/REAXYS Number:
7209267
EC Number:
285-290-9
MDL number:
MFCD00009909
UNSPSC Code:
12352100
PubChem Substance ID:
24855967
NACRES:
NA.22

grade

technical grade

Quality Level

100

assay

80%

form

solid

mp

50-55 °C (lit.)

SMILES string

NCc1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI

1S/C9H7F6N/c10-8(11,12)6-1-5(4-16)2-7(3-6)9(13,14)15/h1-3H,4,16H2

InChI key

DHVHORCFFOSRBP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3,5-Bis(trifluoromethyl)benzylamine has been used in the preparation of phenyl glycine derivatives.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Piperonylamine 97%

Sigma-Aldrich

P49503

Piperonylamine

3,5-Bis(trifluoromethyl)benzaldehyde 97%

Sigma-Aldrich

290130

3,5-Bis(trifluoromethyl)benzaldehyde

Triethylamine ≥99.5%

Sigma-Aldrich

471283

Triethylamine

4-Fluorobenzylamine 97%

Sigma-Aldrich

162493

4-Fluorobenzylamine

2,2,2-Trifluoroethylamine 99.5%

Sigma-Aldrich

269042

2,2,2-Trifluoroethylamine

Toluene anhydrous, 99.8%

Sigma-Aldrich

244511

Toluene

Lihu Yang et al.
Bioorganic & medicinal chemistry letters, 16(14), 3735-3739 (2006-05-16)
Systematic modification of a screening lead yielded a class of potent glycinamide based CCR2 antagonists. The best compound (55, (2S)-N-[3,5-bis(trifluoromethyl)benzyl]-2-{[2-(1-piperidinyl)ethyl]amino}-2-(3-thienyl)acetamide) displayed good binding affinity (IC50=30 and 39 nM) toward human monocytes and CHO cell expressing human CCR2b, respectively. Functionally, it

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