모든 사진(3)
About This Item
실험식(Hill 표기법):
C6H12
CAS Number:
Molecular Weight:
84.16
Beilstein:
1900225
EC Number:
MDL number:
UNSPSC 코드:
12191502
eCl@ss:
39010606
PubChem Substance ID:
NACRES:
NA.21
bp:
80.7 °C (lit.)
vapor pressure:
168.8 mmHg ( 37.7 °C)
77 mmHg ( 20 °C)
77 mmHg ( 20 °C)
가격 및 재고 정보를 현재 이용할 수 없음
추천 제품
일반 설명
Cyclohexane is a cyclic alkane that predominantly exists in chair conformation due to higher stability.[1] It participates as starting reagent in the photonitrosylation process (PNC process) and affords ε-caprolactum.[2] Its oxidation by employing various oxidants such as hydrogen peroxide, tert-butyl hydroperoxide and molecular oxygen has been reported.[3]
애플리케이션
Cyclohexane has been used in the following studies:
Cyclohexane may undergo oxidation using hydrogen peroxide as oxidant and in the presence of a polyoxotungstate catalyst to form cyclohexanone and cyclohexanol as the main products. Its dehydrogenation in the presence of Ni-Cu/SiO2 catalysts forms benzene in good yield.[7]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
-4.0 °F - closed cup
Flash Point (°C)
-20 °C - closed cup
이미 열람한 고객
The energy difference between the chair and boat forms of cyclohexane. The twist conformation of Cyclohexane.
Johnson WS, et al.
Journal of the American Chemical Society, 83(3), 606-614 (1961)
Cyclohexane dehydrogenation over Ni-Cu/SiO 2 catalyst: Effect of copper addition.
Xia Z, et al.
Catalysis Communications, 90, 39-42 (2017)
Samuel Kim et al.
Methods in enzymology, 472, 119-132 (2010-06-29)
Microfluidics serves as a convenient platform for single-molecule experiments by providing manipulation of small amounts of liquids and micron-sized particles. An adapted version of capillary electrophoresis (CE) on a microchip can be utilized to separate chemical species with high resolution
Characterizations and performances of Ni/diatomite catalysts for dry reforming of methane.
Jabbour K, et al.
Chemical Engineering Journal, 264, 351-358 (2015)
Comparison of the triboluminescent yield and decay time for europium dibenzoylmethide triethylammonium synthesized using different solvents.
Fontenot RS, et al.
CrystEngComm, 14(4), 1382-1386 (2012)
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.