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Benzene, 1,1'-(2-bromoethylidene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40231-75-2

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40231-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40231-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40231-75:
(7*4)+(6*0)+(5*2)+(4*3)+(3*1)+(2*7)+(1*5)=72
72 % 10 = 2
So 40231-75-2 is a valid CAS Registry Number.

40231-75-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromoethane-1,1-diyl)dibenzene

1.2 Other means of identification

Product number -
Other names (2-bromo-1-phenylethyl)benzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40231-75-2 SDS

40231-75-2Relevant academic research and scientific papers

An Electron Spin Resonance Investigation of β-Substituted 1,1-Diphenylethyl Radicals

Leardini, Rino,Tundo, Antonio,Zanardi, Giuseppe,Pedulli, Gian Franco

, p. 285 - 290 (1983)

A large number of β-substituted 1,1-diphenylethyl derivatives Ph2C.CH2MRn have been generated by addition of .MRn radicals to 1,1-diphenylethylene.The magnitude of the β-proton hyperfine splitting constants toge

Chemoselective Homologation-Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)-Halomethyl-Alkanes

Citarella, Andrea,Holzer, Wolfgang,Ielo, Laura,Langer, Thierry,Miele, Margherita,Pace, Vittorio,Urban, Ernst,Zehl, Martin

supporting information, p. 7629 - 7634 (2020/10/12)

The sequential installation of a carbenoid and a hydride into a carbonyl, furnishing halomethyl alkyl derivatives, is reported. Despite the employment of carbenoids as nucleophiles in reactions with carbon-centered electrophiles, sp3-type alkyl halides remain elusive materials for selective one-carbon homologations. Our tactic levers on using carbonyls as starting materials and enables uniformly high yields and chemocontrol. The tactic is flexible and is not limited to carbenoids. Also, diverse carbanion-like species can act as nucleophiles, thus making it of general applicability.

Development of dual-acting benzofurans for thromboxane A2 receptor antagonist and prostacyclin receptor agonist: Synthesis, structure-activity relationship, and evaluation of benzofuran derivatives

Ohno, Michihiro,Miyamoto, Mitsuko,Hoshi, Kazuhiro,Takeda, Takahiro,Yamada, Naohiro,Ohtake, Atsushi

, p. 5279 - 5294 (2007/10/03)

Prostacyclin (PGI2) is an unstable, powerful endogenous inhibitor of platelet aggregation, and thromboxane A2 (TXA 2) is an unstable endogenous arachidonic acid metabolite that plays a pivotal role in platelet aggregation and vasoconstriction. The balance between TXA2 and PGI2 greatly affects maintenance of the homeostasis of the circulatory system. A novel series of benzofuran-7- yloxyacetic acid derivatives was discovered as potent dual-acting agents to block the thromboxane A2 receptor and to activate the prostacyclin receptor. Synthesis, structure-activity relationship, and in vitro and ex vivo pharmacology of this series of compounds are described. The most potent in the series was {3-[2-(1,1-diphenylethylsulfanyl)ethyl]-2-hydroxymethylbenzofuran-7- yloxy}acetic acid diethanolamine salt (7) with Ki of 4.5 nM for thromboxane receptor antagonism and Ki of 530 nM for prostacyclin receptor agonism. Remarkably, compound 7 is a promising candidate for novel treatment as an antithrombotic agent with other cardiovascular actions to avoid hypotensive side effects.

Hydroalumination of alkenes by the LiAlH4*3AlBr3 system

Gorobets, E. V.,Shitikova, O. V.,Lomakina, S. I.,Tolstikov, G. A.,Kuchin, A. V.

, p. 1573 - 1578 (2007/10/02)

The hydroalumination of a series of alkenes and some fused aromatic hydrocarbons by the LiAlH4*3AlBr3 system in low-polar solvents was studied.Alkenes with mono-, di-, tri-, and tetraalkyl substituted, mono- and diaryl substituted double bonds and anthracene react at room temperature to give the corresponding dibromoaluminoalkanes in high yields.Benzylidenefluorene, tetraphenylethylene, naphthalene, and phenanthrene do not undergo hydroalumination under these conditions.Camphene, bicyclooct-2-ene, and norbornene afford the corresponding organoaluminum compounds with high stereoselectivity.Oxidation and halo- and acyldemetallation of the resulting alkyl- and arylalanes were carried out.

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