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Merck
CN

260630

tert-Butyl isocyanide

98%

Synonym(s):

1,1-Dimethylethyl isocyanide, 1-tert-Butylisonitrile, 2-Isocyano-2-methylpropane, t-Butylisonitrile, tert-Butylisonitrile

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About This Item

Linear Formula:
(CH3)3CNC
CAS Number:
7188-38-7
Molecular Weight:
83.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24855763
EC Number:
230-553-5
Beilstein/REAXYS Number:
1903156
MDL number:
MFCD00000002
Assay:
98%
Form:
liquid

Key Documents

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InChI key

FAGLEPBREOXSAC-UHFFFAOYSA-N

InChI

1S/C5H9N/c1-5(2,3)6-4/h1-3H3

SMILES string

CC(C)(C)[N+]#[C-]

assay

98%

form

liquid

Quality Level

200

refractive index

n20/D 1.376 (lit.)

bp

91 °C (lit.)

density

0.735 g/mL at 25 °C (lit.)

functional group

amine, isonitrile

Related Categories

General description

Carbon dative bond formation by tert-butyl isocyanide on the germanium (100) surface has been reported. It also forms complexes with metals and inserts into metal-carbon bonds to form iminoacyls.

Application

tert-Butyl isocyanide was used in the synthesis of coumarines, 4H-chromenes and isoxazolines. It was also used to trap 2-cyclopropylidene-1,3-diones.

pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

hcodes

H225,H330

Hazard Classifications

Acute Tox. 2 Inhalation - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

28.4 °F - closed cup

flash_point_c

-2 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ3717
BCCB0126
BCBZ6961
BCBS1379V
BCBM8296V

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Habib Nasri et al.
Inorganic chemistry, 43(9), 2932-2942 (2004-04-27)
The addition of the strongly pi-bonding ligands CO or tert-butyl isocyanide to the low-spin five-coordinate iron(II) nitrite species [Fe(TpivPP)(NO2)]- (TpivPP = picket fence porphyrin) gives two new six-coordinate species [Fe(TpivPP)(NO2)(CO)]- and [Fe(TpivPP)(NO2)(t-BuNC)]-. These species have been characterized by single-crystal structure
Synthesis of coumarines and 4H-chromenes through the reaction of tert-butyl isocyanide and dialkyl acetylenedicarboxylates in presence of 2-hydroxybenzaldehydes.
Yavari I, et al.
Synthesis, 5, 679-682 (2004)
Organometallics, 12, 2414-2414 (1993)
Journal of the Chemical Society. Chemical Communications, 189-189 (1987)
D Bandyopadhyay et al.
Biochemistry, 35(5), 1500-1505 (1996-02-06)
The kinetics of tert-butyl isocyanide binding to the heme protein horseradish peroxidase (HRP) at 22 degrees C was examined on all time scales, from minutes to picoseconds, in aqueous borate buffer at pH 9.08. Unlike myoglobin (Mb) or hemoglobin, HRP
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