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(E)-9-styryl-9H-fluorene is an organic compound characterized by its unique molecular structure, which consists of a fluorene core with a vinyl group attached to the 9-position in the E-configuration. (E)-9-styryl-9H-fluorene is a conjugated molecule, meaning it has alternating single and double bonds, which contribute to its electronic properties. It is often used in the synthesis of advanced materials, such as organic semiconductors and optoelectronic devices, due to its ability to absorb and emit light efficiently. The E-configuration refers to the geometric isomerism around the double bond, where the substituents are on opposite sides of the bond, leading to distinct physical and chemical properties compared to the Z-isomer.

5751-43-9

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5751-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5751-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5751-43:
(6*5)+(5*7)+(4*5)+(3*1)+(2*4)+(1*3)=99
99 % 10 = 9
So 5751-43-9 is a valid CAS Registry Number.

5751-43-9Downstream Products

5751-43-9Relevant academic research and scientific papers

Transition-Metal-Free Stereospecific Cross-Coupling with Alkenylboronic Acids as Nucleophiles

Li, Chengxi,Zhang, Yuanyuan,Sun, Qi,Gu, Tongnian,Peng, Henian,Tang, Wenjun

, p. 10774 - 10777 (2016)

We herein report a transition-metal-free cross-coupling between secondary alkyl halides/mesylates and aryl/alkenylboronic acid, providing expedited access to a series of nonchiral/chiral coupling products in moderate to good yields. Stereospecific SN2-type coupling is developed for the first time with alkenylboronic acids as pure nucleophiles, offering an attractive alternative to the stereospecific transition-metal-catalyzed C(sp2)-C(sp3) cross-coupling.

Metal-free and recyclable route to synthesize polysubstituted olefins via C-C bond construction from direct dehydrative coupling of alcohols or alkenes with alcohols catalyzed by sulfonic acid-functionalized ionic liquids

Han, Feng,Yang, Lei,Li, Zhen,Zhao, Yingwei,Xia, Chungu

, p. 2506 - 2516 (2014/09/17)

A direct synthesis of polysubstituted olefins via construction of C-C bonds, which involves the direct dehydrative coupling of alcohols or alkenes with alcohols, was realized using a series of alkanesulfonic acid group-functionalized ionic liquids (SO3H-functionlization ILs) without additives. The metal-free and recyclable catalyst system avoided the disposal and neutralization of acidic catalysts after reaction and tolerated a broad range of substrates, including benzylic, allyl, propargylic, aliphatic and aromatic or aliphatic olefins. Additionally, the catalytic system was suitable for a gram-scale preparation. Preliminary mechanistic studies indicated that the C-H bond cleavage in this reaction might be involved in the rate-determining step.

Iron-catalyzed stereospecific olefin synthesis by direct coupling of alcohols and alkenes with alcohols

Liu, Zhong-Quan,Zhang, Yuexia,Zhao, Lixing,Li, Zejiang,Wang, Jiantao,Li, Huajie,Wu, Long-Min

supporting information; experimental part, p. 2208 - 2211 (2011/06/20)

Chemical equations presented. An efficient Fe(III)-catalyzed direct coupling of alkenes with alcohols and cross-coupling of alcohols with alcohols to give the corresponding substituted (E)-alkenes stereospecifically is demonstrated. Additionally, this reaction could be scaled up. The kinetic isotope effect (KIE) experiments indicated a typical secondary isotope effect in this process. Although benzylic alcohols were effective substrates, mild conditions, atom efficiency, environmental soundness, and stereospecificity are features that make this procedure very attractive.

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