추천 제품
Quality Level
분석
99%
형태
powder
반응 적합성
reaction type: C-C Bond Formation
mp
≥300 °C (lit.)
SMILES string
[Cl-].C(c1ccccc1)[P+](c2ccccc2)(c3ccccc3)c4ccccc4
InChI
1S/C25H22P.ClH/c1-5-13-22(14-6-1)21-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25;/h1-20H,21H2;1H/q+1;/p-1
InChI key
USFRYJRPHFMVBZ-UHFFFAOYSA-M
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of:
It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites.
- Platinum chloro-tetrazole complexes via azidation.
- Trans-stilbenes and cinnamates via Wittig olefination.
- Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment.
- Pentiptycenes for use as light-driven molecular brakes.
- Archipelago structures for formation of petroleum asphaltenes.
It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites.
Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites
Reactant for synthesis of:
Reactant for formation of archipelago structures for formation of petroleum asphaltenes
Reactant for synthesis of:
- Platinum chloro tetrazole complexes via azidation
- Trans-stilbenes and cinnamates via Wittig olefination
- Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment
- Pentiptycenes for use as light-driven molecular brakes
Reactant for formation of archipelago structures for formation of petroleum asphaltenes
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - STOT RE 1 - STOT SE 3
표적 기관
Lungs,nasal cavity, Respiratory system
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
572.0 °F - closed cup
Flash Point (°C)
300 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
이미 열람한 고객
Synthesis and tyrosinase inhibition activity of trans-stilbene derivatives.
Bioorganic Chemistry, 64, 97-102 (2016)
Pentiptycene?Derived Light?Driven Molecular Brakes: Substituent Effects of the Brake Component.
Chemistry?A European Journal , 16(38), 11594-11604 (2010)
Orally active achiral N-hydroxyformamide inhibitors of ADAM-TS4 (aggrecanase-1) and ADAM-TS5 (aggrecanase-2) for the treatment of osteoarthritis.
Bioorganic & Medicinal Chemistry Letters, 21(11), 3301-3306 (2011)
Tube-like natural halloysite/fluoroelastomer nanocomposites with simultaneous enhanced mechanical, dynamic mechanical and thermal properties.
European Polymer Journal, 47(9), 1746-1755 (2011)
Formation of archipelago structures during thermal cracking implicates a chemical mechanism for the formation of petroleum asphaltenes.
Energy and Fuels, 25(5), 2130-2136 (2011)
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