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线性分子式:
CH3(CH2)5NCS
化学文摘社编号:
分子量:
143.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-549-2
Beilstein/REAXYS Number:
1751837
MDL number:
Assay:
95%
InChI key
WXYAXKKXIGHXDS-UHFFFAOYSA-N
InChI
1S/C7H13NS/c1-2-3-4-5-6-8-7-9/h2-6H2,1H3
SMILES string
CCCCCCN=C=S
assay
95%
refractive index
n20/D 1.493 (lit.)
bp
136-138 °C/96 mmHg (lit.)
density
0.929 g/mL at 25 °C (lit.)
functional group
amine, isothiocyanate
General description
Hexyl isothiocyanate (n-hexyl isothiocyanate) is an isothiocyanate derivative. It has been identified as one of the components present in the oil extracted from the Cruciferae family. On heating the mixture of n-hexyl isothiocyanate and m-chlorophenyl isothiocyanate in the temperature range of 190-230°C, n-hexyl isocyanate is obtained.
Application
Hexyl isothiocyanate may be used as a starting reagent in the synthesis of hexyl isocyanate.
signalword
Danger
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
195.8 °F - closed cup
flash_point_c
91 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
Linskens H-F and Jackson JF.
Gas Chromatography/Mass Spectrometry, Volume 3 of Molecular Methods of Plant Analysis, 265-265 (2012)
Birsa ML, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 134-134 (2014)
Moody CJ.
Comprehensive Organic Functional Group Transformations: Synthesis: carbon with two heteroatoms, each attached by a single bond, 5, 1009-1009 (1995)
Toshiro Noshita et al.
European journal of medicinal chemistry, 44(12), 4931-4936 (2009-09-01)
There is increasing demand for novel anti-inflammatory drugs with different mechanisms of action. We synthesized a series of isothiocyanates 2b-h based on 6-(methylsulfinyl)hexyl isothiocyanate (6-MITC) found in the pungent spice Wasabia japonica. Inhibitory activities against in-vitro growth of tumor cells
Krishna Jayant et al.
Cell reports, 26(1), 266-278 (2019-01-04)
Intracellular recordings in vivo remains the best technique to link single-neuron electrical properties to network function. Yet existing methods are limited in accuracy, throughput, and duration, primarily via washout, membrane damage, and movement-induced failure. Here, we introduce flexible quartz nanopipettes (inner
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