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C105406

Sigma-Aldrich

Cyclohexyl isothiocyanate

98%

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About This Item

Linear Formula:
C6H11NCS
CAS Number:
1122-82-3
Molecular Weight:
141.23
Beilstein:
774525
EC Number:
214-361-9
MDL number:
MFCD00003841
UNSPSC Code:
12352100
PubChem Substance ID:
24891961
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.536 (lit.)

bp

219 °C (lit.)

density

0.996 g/mL at 25 °C (lit.)

SMILES string

S=C=NC1CCCCC1

InChI

1S/C7H11NS/c9-6-8-7-4-2-1-3-5-7/h7H,1-5H2

InChI key

MZSJGCPBOVTKHR-UHFFFAOYSA-N

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Related Categories

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H314,H317,H334

Hazard Classifications

Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

203.0 °F - closed cup

Flash Point(C)

95 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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This paper reports the enhanced performance of cholesterol oxidase (COx) conjugated CdSe/ZnS quantum dots (QDs) by using water-soluble mercaptoacitic acid (MAA) as linker. The functionalized MAA-CdSe/ZnS QDs conjugated in four different dilutions of cholesterol oxidase significantly affected QDs photoluminescence intensities
Peter Ulrich et al.
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Because of emerging resistance to existing drugs, new chemical classes of antimalarial drugs are urgently needed. We have rationally designed a library of compounds that were predicted to accumulate in the digestive vacuole and then decrystallize hemozoin by breaking the
Fazila Rizvi et al.
Scientific reports, 9(1), 6738-6738 (2019-05-03)
A library of thiosemicarbazide derivatives of isoniazid 3-27, was synthesized and evaluated for their anti-inflammatory and urease inhibition activities, by using in vitro bioassays. Among these compounds 9, 10, 12, 21, and 26 were identified as new derivatives. Prolonged use

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