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Merck
모든 사진(1)

문서

475912

Sigma-Aldrich

Hexyl isothiocyanate

95%

동의어(들):

1-Isothiocyanatohexane, n-Hexyl mustard oil

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About This Item

Linear Formula:
CH3(CH2)5NCS
CAS Number:
Molecular Weight:
143.25
Beilstein:
1751837
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

95%

refractive index

n20/D 1.493 (lit.)

bp

136-138 °C/96 mmHg (lit.)

density

0.929 g/mL at 25 °C (lit.)

SMILES string

CCCCCCN=C=S

InChI

1S/C7H13NS/c1-2-3-4-5-6-8-7-9/h2-6H2,1H3

InChI key

WXYAXKKXIGHXDS-UHFFFAOYSA-N

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일반 설명

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.

애플리케이션

Hexyl isothiocyanate may be used as a starting reagent in the synthesis of hexyl isocyanate.

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

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

WGK

WGK 3

Flash Point (°F)

195.8 °F - closed cup

Flash Point (°C)

91 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리 방문

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)
Linskens H-F and Jackson JF.
Gas Chromatography/Mass Spectrometry, Volume 3 of Molecular Methods of Plant Analysis, 265-265 (2012)
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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