추천 제품
Quality Level
분석
≥95% (HPLC)
형태
powder
mp
82-87 °C
저장 온도
−20°C
SMILES string
CSC1=NN=C(SC)N=N1
InChI
1S/C4H6N4S2/c1-9-3-5-7-4(10-2)8-6-3/h1-2H3
InChI key
ROUDTSAXQIBBFZ-UHFFFAOYSA-N
애플리케이션
3,6-Bis(methylthio)-1,2,4,5-tetrazine can be used as a versatile building block in the inverse elecron demand hetero Diels-Alder reactions. The Boger Research Group has reported this powerful approach in the synthesis of alkaloids.
It can also used to synthesize:
It can also used to synthesize:
- Substituted indoles and indolines derivatives by sequential [4+2] cycloaddition reactions.
- 3-(Methylthio)-6-(4-morpholinyl)-1,2,4,5-tetrazine by aromatic nucleophilic substitution reaction.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
3, 6-Diphenyl-1, 2, 4, 5-tetrazine
Encyclopedia of Reagents for Organic Synthesis, Second Edition, 65(26), 9120-9124 (2001)
Triphenylamine/tetrazine based ?-conjugated systems as molecular donors for organic solar cells
New. J. Chem., 39(12), 9700-9713 (2015)
Total synthesis of Amaryllidaceae alkaloids utilizing sequential intramolecular heterocyclic azadiene Diels- Alder reactions of an unsymmetrical 1, 2, 4, 5-tetrazine
The Journal of Organic Chemistry, 65(26), 9120-9124 (2000)
문서
The inverse electron demand Diels-Alder reactions of electron-deficient heterocycles are significant cycloaddition reactions for the total synthesis of natural products containing highly substituted and functionalized heteroaromatic ring systems.
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