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Merck
모든 사진(1)

주요 문서

141070

Sigma-Aldrich

Isopropyl isocyanate

≥98%

동의어(들):

1-Methylethyl isocyanate, 2-Isocyanatopropane, Isopropyl isocyanate, Methyl ethyl isocyanate, Propan-2-yl isocyanate, n-Isopropyl isocyanate

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About This Item

Linear Formula:
(CH3)2CHNCO
CAS Number:
Molecular Weight:
85.10
Beilstein:
969356
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥98%

양식

liquid

refractive index

n20/D 1.382 (lit.)

bp

74-75 °C (lit.)

density

0.866 g/mL at 25 °C (lit.)

작용기

amine
isocyanate

저장 온도

2-8°C

SMILES string

CC(C)N=C=O

InChI

1S/C4H7NO/c1-4(2)5-3-6/h4H,1-2H3

InChI key

GSLTVFIVJMCNBH-UHFFFAOYSA-N

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애플리케이션

Isopropyl isocyanate was used as reagent during the synthesis of O-aryl N-isopropylcarbamates. It was used as derivatization reagent during the stereoisomeric analysis of secondary alcohols.

픽토그램

FlameSkull and crossbonesHealth hazard

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 1 Inhalation - Eye Irrit. 2 - Flam. Liq. 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 1

Flash Point (°F)

26.6 °F - closed cup

Flash Point (°C)

-3 °C - closed cup

개인 보호 장비

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


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Matthias Kauch et al.
The Journal of organic chemistry, 70(18), 7149-7158 (2005-08-27)
[reaction: see text] Herein we report regioselective substitution reactions of a series of 2- and 3-hydroxybiaryls including BINOL via a new directed ortho-metalation procedure. O-Aryl N-isopropylcarbamates, conveniently prepared from phenols and isopropyl isocyanate, are temporarily and in situ N-protected by
Joakim Bång et al.
Journal of chemical ecology, 37(1), 125-133 (2010-11-27)
A GC-MS method to analyze the stereoisomeric composition of chiral secondary alcohols found in whole body extracts of pine sawfly females was developed. The tested alcohols were derivatized with optically pure (S)-2-acetoxypropionyl chloride prior to GC-MS analysis. Baseline separation was

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