추천 제품
분석
98%
형태
crystals
bp
350 °C (lit.)
mp
150-152 °C (lit.)
SMILES string
c1ccc(cc1)\C=C\C=C\c2ccccc2
InChI
1S/C16H14/c1-3-9-15(10-4-1)13-7-8-14-16-11-5-2-6-12-16/h1-14H/b13-7+,14-8+
InChI key
JFLKFZNIIQFQBS-FNCQTZNRSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
애플리케이션
trans,trans-1,4-Diphenyl-1,3-butadiene can be used as a reactant to synthesize:
It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.
- 2,5-diphenylthiophene by oxidation reaction with potassium sulfide and DMSO.
- 2-[(3E)-4-Phenyl-2-(phenylmethyl)-3-buten-1-yl]furan via nickel catalyzed hydrobenzylation reaction with furfural in the presence of N2H4.
It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.
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
개인 보호 장비
dust mask type N95 (US), 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.
Nickel-catalyzed regioselective hydrobenzylation of 1, 3-dienes with hydrazones
ACS Catalysis, 9(10), 9199-9205 (2019)
Organic letters, 20(23), 7392-7395 (2018-11-22)
A novel, atom economical, and transition-metal-free strategy for the synthesis of thiophenes from substituted buta-1-enes with potassium sulfide has been presented. The reaction achieves double C-S bond formations via cleavage of multiple C-H bonds and provides an efficient approach to
Syntheses and structural studies on silver (I) coordination polymers with trans, trans-1, 4-dipenyl-1, 3-butadiene
Inorganica chimica acta, 342, 202-208 (2003)
PloS one, 10(5), e0125342-e0125342 (2015-05-06)
Pathogen-specific and overall infection burden may contribute to atherosclerosis and cardiovascular disease (CVD), but the effect of infection severity and timing is unknown. We investigated whether childhood infection-related hospitalisation (IRH, a marker of severity) was associated with subsequent adult CVD
Bioorganic & medicinal chemistry letters, 15(20), 4438-4446 (2005-09-03)
Monoamine oxidase (EC1.4.3.4; MAO) is a mitochondrial outer membrane flavoenzyme that catalyzes the oxidation of biogenic amines. It has two distinct isozymic forms designated MAO-A and MAO-B, each displaying different substrate and inhibitor specificities. They are the well-known targets for
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