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化驗
97%
折射率
n20/D 1.493 (lit.)
bp
29-30 °C/10 mmHg (lit.)
密度
0.948 g/mL at 25 °C (lit.)
SMILES 字串
CC(C)N=C=S
InChI
1S/C4H7NS/c1-4(2)5-3-6/h4H,1-2H3
InChI 密鑰
VHBFEIBMZHEWSX-UHFFFAOYSA-N
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一般說明
Isopropyl isothiocyanate is an isothiocyanate derivative. It has been identified as one of the volatile components in the following:
Molecular conformations of isopropyl isothiocyanate in gas phase have been determined by electron diffraction studies. It has been synthesized by employing isopropyl amine as a starting reagent.
- seed kernel and leaf of Moringa peregrina (Forssk.) Fiori, Agricolt1
- essential oil isolated from Upland Wasabi
- hydrodistillates of hedge mustard (Sysimbrium officinale)
Molecular conformations of isopropyl isothiocyanate in gas phase have been determined by electron diffraction studies. It has been synthesized by employing isopropyl amine as a starting reagent.
應用
Isopropyl isothiocyanate may be used to synthesize 4-bromo-5,6-dichloro-2-isopropylaminobenzimidazole.
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
104.0 °F - closed cup
閃點（°C）
40 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
A general and facile one-pot process of isothiocyanates from amines under aqueous conditions.
Sun N, et al.
Beilstein Journal of Organic Chemistry, 8(1), 61-70 (2012)
Synthesis and antiviral evaluation of halogenated ?-d-and-l-erythrofuranosylbenzimidazoles.
Gudmundsson KS, et al.
Journal of Medicinal Chemistry, 43(12), 2464-2472 (2000)
Analysis of volatile components in essential oil of upland wasabi and their inhibitory effects on platelet aggregation.
Kumagai H, et al.
Bioscience, Biotechnology, and Biochemistry, 58(12), 2131-2135 (1994)
Ivica Blazević et al.
Chemistry & biodiversity, 7(8), 2023-2034 (2010-08-24)
Volatile compounds of hedge mustard (Sysimbrium officinale) have been investigated for the first time. Forthy-two compounds were identified after hydrodistillation (without or upon autolysis) after gas chromatography and gas chromatography/mass spectrometry analyses. In addition, after decoction and hydrolysis of O-glycosides
Electron diffraction investigation of the molecular structures of isopropyl isocyanate and isopropyl isothiocyanate.
Cradock S, et al.
Journal of Molecular Structure, 140(3), 199-207 (1986)
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