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Merck
CN

196878

3-(Trifluoromethyl)benzaldehyde

97%

Synonym(s):

α,α,α-Trifluoro-m-tolualdehyde

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About This Item

Linear Formula:
CF3C6H4CHO
CAS Number:
454-89-7
Molecular Weight:
174.12
Beilstein:
2327537
EC Number:
207-228-1
MDL number:
MFCD00003373
UNSPSC Code:
12352100
PubChem Substance ID:
24851803
NACRES:
NA.22

Key Documents

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Quality Level

100

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
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H410

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4431
SDBB0649
STBK5506
STBJ1666
STBH7125

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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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