모든 사진(3)
About This Item
Linear Formula:
C6H5CN
CAS Number:
Molecular Weight:
103.12
Beilstein:
506893
EC Number:
MDL number:
UNSPSC 코드:
12352002
eCl@ss:
39031505
PubChem Substance ID:
NACRES:
NA.21
Grade:
anhydrous
분석:
≥99%
bp:
191 °C (lit.)
추천 제품
Grade
anhydrous
Quality Level
분석
≥99%
양식
liquid
expl. lim.
0.34-6.3 %
불순물
<0.003% water
<0.005% water (100 mL pkg)
증발 잔류물
<0.0003%
refractive index
n20/D 1.528 (lit.)
bp
191 °C (lit.)
mp
−13 °C (lit.)
SMILES string
N#Cc1ccccc1
InChI
1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H
InChI key
JFDZBHWFFUWGJE-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Benzonitrile may be used in the synthesis of organic building blocks such as 2-cyclopentylacetophenone, 4-carbomethoxy-5-methoxy-2-phenyl-1,3-oxazole and 1-phenyl-3,4-dihydro-6,7-methylenedioxyisoquinoline. It may also be used as a solvent in the synthesis of bis(trifluoromethyl)diazomethane.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
Flash Point (°F)
158.0 °F - closed cup
Flash Point (°C)
70 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
이미 열람한 고객
Rhodium-catalyzed heterocycloaddition of a diazomalonate and a nitrile: 4-carbomethoxy-5-methoxy-2-phenyl-1,3-oxazole
Tullis JS and Helquist P
Organic Syntheses, 74, 229-229 (1997)
Bis(trifluoromethyl)diazomethane
Middleton WJ and Gale DM
Organic Syntheses, 50, 6-6 (1970)
Generation and cyclization of 5-hexenyllithium: 2-cyclopentylacetophenone
Bailey WF, et al
Organic Syntheses, 81, 121-121 (2005)
Microwave spectra of isotopic benzonitriles. Refined molecular structure of benzonitrile.
Casado J, et al.
Journal of Molecular Structure, 8(1-2), 211-224 (1971)
Kenji Ueura et al.
Organic letters, 7(11), 2229-2231 (2005-05-20)
[reaction: see text]. The Suzuki-Miyaura-type cross-coupling of arylboron compounds with aryl halides proceeds efficiently in the presence of a rhodium-based catalyst system to produce the corresponding biaryls. Furthermore, it has unexpectedly been observed that the treatment with benzonitrile under similar
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