73478
Nitromethane
puriss., absolute, over molecular sieve, ≥98.5% (GC)
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
CH3NO2
CAS 번호:
Molecular Weight:
61.04
Beilstein:
1698205
EC Number:
MDL number:
UNSPSC 코드:
12352102
PubChem Substance ID:
NACRES:
NA.21
Bp:
101.2 °C (lit.)
Vapor pressure:
2.7 mmHg
vapor density
2.1 (vs air)
Quality Level
vapor pressure
2.7 mmHg
grade
absolute
puriss.
분석
≥98.5% (GC)
양식
liquid
autoignition temp.
784 °F
품질
over molecular sieve
expl. lim.
7.3 %, 33 °F
기술
GC/GC: suitable
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
The catalytic chemistry of nitromethane over Co-ZSM5 and other catalysts in connection with the methane-NOxSCR reaction.
Cowan AD, et al.
J. Catal., 176(2), 329-343 (1998)
Metal ion encapsulation: cobalt cages derived from polyamines, formaldehyde, and nitromethane.
Geue RJ, et al.
Journal of the American Chemical Society, 106(19), 5478-5488 (1984)
Benedek Vakulya et al.
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.
Atanu Bhattacharya et al.
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
Eagleson M.
Concise Encyclopedia Chemistry, 696-696 (1994)
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