Skip to Content
Merck
CN
All Photos(1)

Documents

196878

Sigma-Aldrich

3-(Trifluoromethyl)benzaldehyde

97%

Sign Into View Organizational & Contract Pricing

Synonym(s):
α,α,α-Trifluoro-m-tolualdehyde
Linear Formula:
CF3C6H4CHO
CAS Number:
Molecular Weight:
174.12
Beilstein:
2327537
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.465 (lit.)

bp

83-86 °C/30 mmHg (lit.)

density

1.301 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1cccc(c1)C(F)(F)F

InChI

1S/C8H5F3O/c9-8(10,11)7-3-1-2-6(4-7)5-12/h1-5H

InChI key

NMTUHPSKJJYGML-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Aldol reaction of 3-(trifluoromethyl)benzaldehyde with hydroxyacetone in the aldolase antibody 38C2-ionic liquid system has been investigated.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Synthesis of fluorinated materials catalyzed by proline or antibody 38C2 in ionic liquid.
Kitazume T, et al.
Journal of Fluorine Chemistry, 121(2), 205-212 (2003)
Kazuhiro Takano et al.
Development, growth & differentiation, 53(1), 37-47 (2011-01-26)
This study investigated the development of Ca²(+) signaling mechanisms and their role in initiating morphogenetic cell movement in the presumptive ectoderm of Japanese newt (Cynops pyrrhogaster) during gastrulation. Histochemical staining using fluorescently labeled ryanodine and dihydropyridine probes revealed that dihydropyridine

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