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Key Documents

196878

Sigma-Aldrich

3-(Trifluoromethyl)benzaldehyde

97%

Synonym(s):

α,α,α-Trifluoro-m-tolualdehyde

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About This Item

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.)

functional group

aldehyde
fluoro

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

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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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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

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