추천 제품
vapor pressure
1.4 mmHg ( 20 °C)
Quality Level
분석
≥98%
양식
liquid
refractive index
n20/D 1.535 (lit.)
bp
162-163 °C (lit.)
mp
−30 °C (lit.)
density
1.096 g/mL at 25 °C (lit.)
작용기
isocyanate
저장 온도
2-8°C
SMILES string
O=C=Nc1ccccc1
InChI
1S/C7H5NO/c9-6-8-7-4-2-1-3-5-7/h1-5H
InChI key
DGTNSSLYPYDJGL-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Phenyl isocyanate reacts with ethyl alcohol to yield ethyl α,γ-diphenylallophanate and trace of phenyl isocyanate dimer.
애플리케이션
Phenyl isocyanate (PhNCO) can undergo addition reaction with primary nitroparaffins in the presence of a tertiary alkyl amine catalyst to form sym-disubstituted urea and furoxane. It can also react with cyclohexadienones to form vicinal diamine-containing heterocycle derivatives.
Phenyl isocyanate was used to prepare chemically modified cellulose paper. It was used in the synthesis of functionalized graphene oxide nanoplatelets.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Corr. 1C - Skin Sens. 1A - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
123.8 °F - closed cup
Flash Point (°C)
51 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
DBU-Catalyzed Desymmetrization of Cyclohexadienones: Access to Vicinal Diamine-Containing Heterocycles
Organic Letters, 20(16), 5006-5009 (2018)
The Reactions of Primary Nitroparaffins with Isocyanates1
Journal of the American Chemical Society, 82(20), 5339-5342 (1960)
New Reactions of Phenyl Isocyanate and Ethyl Alcohol1.
Journal of the American Chemical Society, 78(19), 4911-4914 (1956)
Organic & biomolecular chemistry, 10(35), 7070-7077 (2012-08-08)
In mass spectrometry of protonated N-phenylcinnamides, the carbonyl oxygen is the thermodynamically most favorable protonation site and the added proton is initially localized on it. Upon collisional activation, the proton transfers from the carbonyl oxygen to the dissociative protonation site
The Journal of biological chemistry, 264(16), 9300-9303 (1989-06-05)
A new hydroxylated, very long-chain fatty acid has been isolated and characterized from the lipopolysaccharide (LPS) of Rhizobium trifolii ANU 843. The lipid A of the organism was degraded by mild alkali and borohydride and the products methylated, peracetylated, and
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