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Merck
모든 사진(1)

주요 문서

E33300

Sigma-Aldrich

Ethyl isocyanate

98%

동의어(들):

Isocyanatoethane

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About This Item

Linear Formula:
C2H5NCO
CAS Number:
Molecular Weight:
71.08
Beilstein:
773743
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

4.34 psi ( 20 °C)

Quality Level

분석

98%

refractive index

n20/D 1.381 (lit.)

bp

60 °C (lit.)

density

0.898 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

CCN=C=O

InChI

1S/C3H5NO/c1-2-4-3-5/h2H2,1H3

InChI key

WUDNUHPRLBTKOJ-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Ethyl isocyanate undergoes trimerization at high temperature for the synthesis of Isocyanurates.

애플리케이션

Ethyl isocyanate may be used to generate thermoresponsiveness in polyglycidol via partial hydrophobic modification. The poly(glycidol-co-ethyl glycidyl carbamate) thus formed can undergo photocrosslinking in the presence of a photosensitizer to form thermoresponsive gels. It can also be used in the synthesis of 4,5,6,7-tetrahydrobenzo[1,2-d]thiazole-2,6-diamine derivatives that are potent DNA gyrase inhibitors.

신호어

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Repr. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

14.0 °F - closed cup

Flash Point (°C)

-10 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

The synthesis of isocyanurates on the trimerization of isocyanates under high pressure
Taguchi Y, et al.
Bulletin of the Chemical Society of Japan, 63, 3486-3489 (1990)
Design, synthesis, and biological evaluation of 1?ethyl?3?(thiazol?2?yl) urea derivatives as Escherichia coli DNA gyrase inhibitors.
Tomasic T
Arch. Pharm. (Weinheim), 351(1) (2018)
Farid M Sroor et al.
Archiv der Pharmazie, 353(10), e2000069-e2000069 (2020-07-14)
Ethyl 2-acrylamido-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate as well as its corresponding bis-derivatives, 5-10, with aliphatic linkers were synthesized, fully characterized, and tested as novel anticancer agents. The targeted compounds, 5-10, were obtained by the Knoevenagel condensation reactions of bis-o- or -p-aldehyde with a molar
Photocrosslinking Of Polyglycidol And Its Derivative?Route To Thermoresponsive Hydrogels.
Utrata?Wesolek A
Photochemistry and Photobiology, 94(1), 52?60-52?60 (2017)
M Boutin et al.
Journal of occupational and environmental hygiene, 2(9), 456-461 (2005-08-11)
During the thermal degradation of 1,6-hexamethylenediiso- cyanate-based (HDI) car paint, the eight most abundant isocyanates generated are isocyanic acid, methyl isocyanate, ethyl isocyanate, propyl isocyanate, butyl isocyanate, pentyl isocyanate, hexyl isocyanate, and 1,6-hexamethylenediisocyanate. For the first time, a method using

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