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374857

3,5-Bis(trifluoromethyl)phenyl isocyanate

98%

Synonym(s):

1-Isocyanato-3,5-bis(trifluoromethyl)benzene, 3,5-Di(trifluoromethyl)phenyl isocyanate

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About This Item

Linear Formula:
(CF3)2C6H3NCO
CAS Number:
16588-74-2
Molecular Weight:
255.12
NACRES:
NA.22
PubChem Substance ID:
24863344
UNSPSC Code:
12352100
MDL number:
MFCD00013559

Key Documents

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Product Name

3,5-Bis(trifluoromethyl)phenyl isocyanate, 98%

InChI

1S/C9H3F6NO/c10-8(11,12)5-1-6(9(13,14)15)3-7(2-5)16-4-17/h1-3H

SMILES string

FC(F)(F)c1cc(cc(c1)C(F)(F)F)N=C=O

InChI key

NRSSOFNMWSJECS-UHFFFAOYSA-N

assay

98%

form

liquid

refractive index

n20/D 1.43 (lit.)

density

1.476 g/mL at 25 °C (lit.)

functional group

fluoro
isocyanate

Quality Level

100

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3,5-Bis(trifluoromethyl)phenyl isocyanate 98%

Sigma-Aldrich

374857

3,5-Bis(trifluoromethyl)phenyl isocyanate

3,5-Bis(trifluoromethyl)phenyl isothiocyanate 98%

Sigma-Aldrich

468517

3,5-Bis(trifluoromethyl)phenyl isothiocyanate

3,5-Bis(trifluoromethyl)phenylacetonitrile 98%

Sigma-Aldrich

263427

3,5-Bis(trifluoromethyl)phenylacetonitrile

Pentyl isocyanate 98%

Sigma-Aldrich

389951

Pentyl isocyanate

assay

98%

assay

98%

assay

98%

assay

98%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

1.476 g/mL at 25 °C (lit.)

density

1.485 g/mL at 25 °C (lit.)

density

1.42 g/mL at 25 °C (lit.)

density

0.878 g/mL at 25 °C (lit.)

refractive index

n20/D 1.43 (lit.)

refractive index

n20/D 1.5 (lit.)

refractive index

n20/D 1.4234 (lit.)

refractive index

n20/D 1.414 (lit.)

form

liquid

form

-

form

liquid

form

liquid

functional group

fluoro

functional group

fluoro, isothiocyanate

functional group

fluoro, nitrile

functional group

amine, isocyanate

Application

3,5-Bis(trifluoromethyl)phenyl isocyanate may be used in following studies:
  • Chemical derivatization of amino-functionalized model surfaces.[1]
  • Preparation of arylaminothiocarbonylpyridinium zwitterionic salts, via an exothermic reaction with 4-pyrrolidinopyridine.[2]
  • Synthesis of (S)-3-hydroxymethyl-2-methoxymethoxy-2′-(3-(3,5-bis(trifluoromethyl)phenyl)uryl-benzyl)-1,10-binaphthalene.[3]
  • Synthesis of 1-[3,5-bis(trifluoromethyl) phenyl]-3-(2-pyridyl)thiourea, via reaction with 2-amino pyridine in MeCN.[4]

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR2201
SHBR1503
15527LOV
15527LO
16412HR

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Utsab Manna et al.
Dalton transactions (Cambridge, England : 2003), 46(35), 11956-11969 (2017-08-31)
A rationally designed ortho-phenylenediamine based trifluoromethyl meta-disubstituted bis-urea receptor (L) exhibits effective, consistent and systematic binding in its neutral form towards smaller spherical halides (fluoride, chloride, bromide and iodide), and relatively larger planar carbonate and tetrahedral sulphate oxyanions. All the
Huadong Yue et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 5), o858-o858 (2008-01-01)
The title compound, C(14)H(9)F(6)N(3)S, exhibits a nearly planar conformation in the solid state, with a dihedral angle between the planes of the benzene and pyridine rings of 14.86 (3)°. The pyridine N atom allows for the formation of a six-membered N-H⋯N(py)
Kazuaki Ishihara et al.
Organic letters, 10(11), 2187-2190 (2008-04-30)
The exothermic reaction of 3,5-bis(trifluoromethyl)phenyl or 4-nitrophenyl isothiocyanate with 4-pyrrolidinopyridine (PPY) gave the corresponding arylaminothiocarbonylpyridinium salts in quantitative yields. These novel zwitterionic salts were effective as organocatalysts for the transesterification reaction of an equimolar mixture of methyl carboxylates and alcohols
Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors.
Nandhakumar R, et al.
Tetrahedron, 64(33), 7704-7708 (2008)
Biao Wang et al.
The Science of the total environment, 710, 135512-135512 (2019-12-02)
The excessive use of acetochlor (ACT), a commonly used herbicide with latent endocrine disrupting functions, causes surface water pollution. The efficient removal of ACT from contaminated water supplies is of paramount importance. In the current work, 3,5-Bis(trifluoromethyl)phenyl isocyanate (BTP) was
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