추천 제품
분석
99%
형태
liquid
반응 적합성
reaction type: C-C Bond Formation
refractive index
n20/D 1.497 (lit.)
bp
106-108 °C/1 mmHg (lit.)
density
1.095 g/mL at 25 °C (lit.)
SMILES string
CCOP(=O)(Cc1ccccc1)OCC
InChI
1S/C11H17O3P/c1-3-13-15(12,14-4-2)10-11-8-6-5-7-9-11/h5-9H,3-4,10H2,1-2H3
InChI key
AIPRAPZUGUTQKX-UHFFFAOYSA-N
애플리케이션
Reactant for synthesis of:
Reactant for:
- 3,5-dihydroxy-4-isopropylstilbene for treatment of skin disorders
- Natural cytotoxic marine products of polyketide origin via intramolecular Diels-Alder reactions
- Stilbenes via on-column oxidation of vicinal diols and Horner-Emmons reactions
- Inhibitors of teh Wnt pathway for colon cancer repression using Wadsworth-Emmons reactions
- Antimalarial drug analogs against P. falciparum
Reactant for:
- Cyclization of aryl ethers, amines, and amides
- Investigating the effects of functional groups on the performance of clue organic LEDs
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Polymers, 12(8) (2020-08-17)
As a part of our ongoing investigations on passively fire protecting polymeric materials, we have been employing both reactive and additive routes involving phosphorus-containing compounds. These included inorganic and organic substances, and in the latter case, the phosphorus-bearing groups differed
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 18(9), 2174-2179 (2019-05-28)
cis,trans-1,2-Dideuterio-1,4-diphenyl-1,3-butadiene (ct-DPBd2) was synthesized and its cis-trans photoisomerization in cyclohexane-d12 (C6D12) at room temperature was monitored by 1H NMR spectroscopy. The results reveal formation of only trans,trans-1,2-dideuterio-1,4-diphenyl-1,3-butadiene (tt-DPBd2). The failure to detect formation of trans,cis-1,2-dideuterio-1,4-diphenyl-1,3-butadiene (tc-DPBd2) eliminates the possibility that
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