추천 제품
Quality Level
분석
95%
양식
liquid
refractive index
n20/D 1.519 (lit.)
bp
116-117 °C (lit.)
density
0.888 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
C1C=CC=CC=C1
InChI
1S/C7H8/c1-2-4-6-7-5-3-1/h1-6H,7H2
InChI key
CHVJITGCYZJHLR-UHFFFAOYSA-N
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일반 설명
Contains 0.02%-0.15% BHT
애플리케이션
Cycloheptatriene can be used as a reactant to synthesize:
- 2-Hydroxyazulene via [2+2] cycloaddition reaction with dichloroketene, and subsequent ring expansion reaction with diazomethane.
- 7-Alkyl-bicyclo[4.2.1]nona-2,4,7-trienes by cobalt catalyzed [6+2] cycloaddition with terminal alkynes.
- (3,5-Cycloheptadienyl)diphenylphosphine ligand by reacting with diphenylphosphine.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
41.0 °F
Flash Point (°C)
5 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Michael H Palmer et al.
The Journal of chemical physics, 153(5), 054301-054301 (2020-08-11)
The vacuum ultraviolet (VUV) spectrum for cyclohepta-1,3,5-triene up to 10.8 eV shows several broad bands, which are compared with electron impact spectra. Local curve fitting exposed groups of sharp vibrational peaks, which are assigned to Rydberg states. The vertical excitation
(Cycloheptadienyl) diphenylphosphine: A Versatile Hybrid Ligand
Massard A, et al.
Organometallics, 31(3), 947-958 (2012)
Mathieu Achard et al.
Organic letters, 7(12), 2353-2356 (2005-06-04)
[reaction: see text] The CoI2(dppe)/Zn/ZnI2 system effectively catalyzes the [6 + 2] cycloaddition of cycloheptatriene with terminal alkynes to afford 7-alkyl-bicyclo[4.2.1]nona-2,4,7-trienes in fair to excellent yields. The catalyst proved to be tolerant toward functional groups such as ketone, sulfone, ester
[2+ 2] Cycloaddition reaction of cycloheptatriene with dichloroketene. A novel and efficient synthetic strategy for the synthesis of 2-hydroxyazulene
Yokoyama R, et al.
Journal of the Chemical Society. Perkin Transactions 1, (18), 2257-2261 (2001)
Katharina Thum et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 27(7), 2513-2522 (2020-11-17)
The first intermolecular early main group metal-alkene complexes were isolated. This was enabled by using highly Lewis acidic Mg centers in the Lewis base-free cations (Me BDI)Mg+ and (tBu BDI)Mg+ with B(C6 F5 )4 - counterions (Me BDI=CH[C(CH3 )N(DIPP)]2
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