추천 제품
vapor density
2.1 (vs air)
vapor pressure
2.7 mmHg
grade
absolute
puriss.
분석
≥98.5% (GC)
형태
liquid
autoignition temp.
784 °F
품질
over molecular sieve
expl. lim.
7.3 %, 33 °F
불순물
≤0.01% water
water
refractive index
n20/D 1.382 (lit.)
n20/D 1.382
pH
6.4 (20 °C, 0.01 g/L)
bp
101.2 °C (lit.)
mp
−29 °C (lit.)
density
1.127 g/mL at 25 °C (lit.)
SMILES string
C[N+]([O-])=O
InChI
1S/CH3NO2/c1-2(3)4/h1H3
InChI key
LYGJENNIWJXYER-UHFFFAOYSA-N
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일반 설명
Nitromethane is an aliphatic nitro compound. It undergoes Michael addition reaction with chalcones in the presence of cinchona alkaloid-derived chiral bifunctional thiourea organocatalyst. Its conversion to N2 in the presence of Co-ZSM5 (Zeolite Socony Mobil-5) has been studied.
애플리케이션
Nitromethane may be employed in the preparation of cobalt cage complexes.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 3 - Repr. 2
Storage Class Code
4.1A - Other explosive hazardous materials
WGK
WGK 2
Flash Point (°F)
95.0 °F - closed cup
Flash Point (°C)
35 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
The catalytic chemistry of nitromethane over Co-ZSM5 and other catalysts in connection with the methane-NOxSCR reaction.
J. Catal., 176(2), 329-343 (1998)
Metal ion encapsulation: cobalt cages derived from polyamines, formaldehyde, and nitromethane.
Journal of the American Chemical Society, 106(19), 5478-5488 (1984)
Organic letters, 7(10), 1967-1969 (2005-05-07)
Cinchona alkaloid-derived chiral bifunctional thiourea organocatalysts were synthesized and applied in the Michael addition between nitromethane and chalcones with high ee and chemical yields.
The Journal of chemical physics, 136(2), 024321-024321 (2012-01-21)
Decomposition of electronically excited nitro-containing molecules with different X-NO(2) (X = C, N, O) moieties has been intensively investigated over the past decades; however, their decomposition behavior has not previously been compared and contrasted. Comparison of their unimolecular decomposition behavior
Concise Encyclopedia Chemistry, 696-696 (1994)
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