295086
trans-2-Butene
≥99%
동의어(들):
β-trans-Butylene, (2E)-2-Butene, (E)-2-Butene, 2-trans-Butene, 2-trans-Butylene, E-Butene, trans-1,2-Dimethylethylene, trans-2-Butylene, trans-Butene
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모든 사진(1)
About This Item
Linear Formula:
CH3CH=CHCH3
CAS Number:
Molecular Weight:
56.11
Beilstein:
1718756
EC Number:
MDL number:
UNSPSC 코드:
12142100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
애플리케이션
trans-2-Butene can be used as a monomer unit to produce high molecular weight polyolefins with well-defined microstructures by nickle-catalyzed polymerization reaction. It is also used as a reactant in the isomerization reaction to produce the corresponding isomer using acid-activated catalysts.
포장
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
법적 정보
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
또한 이 제품과 함께 일반적으로 구입
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설명
가격
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
Storage Class Code
2A - Gases
WGK
WGK 3
Flash Point (°F)
-4.0 °F - closed cup
Flash Point (°C)
-20 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves
Ni (II)-catalyzed polymerization of trans-2-butene
Leatherman MD and Brookhart M
Macromolecules, 34(9), 2748-2750 (2001)
T Sawamura et al.
Radiation protection dosimetry, 103(2), 117-124 (2003-02-21)
A device able to trap a liquid droplet in a host liquid in a metastable (superheated) state was developed for a better understanding of the operational principles and for an extension of the application of superheated drop detectors (SDDs). Droplets
Fumitoshi Shibahara et al.
Bioorganic & medicinal chemistry letters, 12(14), 1825-1827 (2002-06-28)
A new class of polymer-supported (R,S)-BINAPHOS 1e in which the parent BINAPHOS has two alkoxy-substituents at the 3-positions of the phenyls, has been synthesised. Using its Rh(I) complex, asymmetric hydroformylation of olefins proceeded with higher enantioselectivity in some cases compared
Franz Worek et al.
Archives of toxicology, 86(9), 1379-1386 (2012-03-23)
The reactivation of organophosphorus compound (OP)-inhibited acetylcholinesterase (AChE) by oximes is inadequate in case of different OP nerve agents. This fact led to the synthesis of numerous novel oximes by different research groups in order to identify more effective reactivators.
Philip T M Carlsson et al.
Physical chemistry chemical physics : PCCP, 14(45), 15637-15640 (2012-10-24)
Recent studies have suggested that the reaction of stabilised Criegee Intermediates (CIs) with sulfur dioxide (SO(2)), leading to the formation of a carbonyl compound and sulfur trioxide, is a relevant atmospheric source of sulfuric acid. Here, the significance of this
프로토콜
2-Butene; 2-Methylbutane; 1,3-Butadiene; Propyne
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