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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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851803
EC Number:
207-228-1
Beilstein/REAXYS Number:
2327537
MDL number:
MFCD00003373
Assay:
97%
Form:
liquid

Key Documents

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InChI key

NMTUHPSKJJYGML-UHFFFAOYSA-N

InChI

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

SMILES string

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

assay

97%

form

liquid

Quality Level

100

bp

83-86 °C/30 mmHg (lit.)

density

1.301 g/mL at 25 °C (lit.)

functional group

aldehyde, fluoro

Related Categories

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7619
SDBB4431
SDBB0649
STBK5506
STBJ1666

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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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