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2,2-Dibrom-1-cyclohexyl-cyclopropan, also known as 2,2-dibromocyclohexylcyclopropane, is a chemical compound with the molecular formula C9H14Br2. It is a brominated cyclopropane derivative, featuring a cyclopropane ring fused to a cyclohexane ring, with two bromine atoms attached to the cyclohexane ring. 2,2-Dibrom-1-cyclohexyl-cyclopropan is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of various organic compounds. It is typically synthesized through the reaction of cyclohexene with dibromocarbene, a highly reactive intermediate. The compound's properties, such as its reactivity and stability, make it a valuable building block in the preparation of complex organic molecules, particularly in the fields of pharmaceuticals and agrochemicals.

7087-57-2

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7087-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7087-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7087-57:
(6*7)+(5*0)+(4*8)+(3*7)+(2*5)+(1*7)=112
112 % 10 = 2
So 7087-57-2 is a valid CAS Registry Number.

7087-57-2Relevant academic research and scientific papers

Nickel-catalyzed ring-opening hydroacylation of methylenecyclopropanes: Synthesis of γ,δ-unsaturated ketones from aldehydes

Taniguchi, Hiroki,Ohmura, Toshimichi,Suginome, Michinori

, p. 11298 - 11299 (2009)

(Chemical Equation Presented) A nickel-catalyzed intermolecular hydroacylation of methylenecyclopropanes (MCPs) has been developed. The reaction proceeds with stereospecific cleavage of the proximal C-C bond of the cyclopropane ring to give γ,δ-unsaturate

Copper(ii)-catalyzed protoboration of allenes in aqueous media and open air

Nekvinda, Jan,Santos, Webster L.,Snead, Russell F.

supporting information, p. 14925 - 14931 (2021/09/04)

A method has been developed for the facile Cu(ii)-catalyzed protoboration of monosubstituted allenes in aqueous media under atmospheric conditions. The reaction occurs site selectively, favoring internal alkene protoboration to afford 1,1-disubstituted vinylboronic acid derivatives (up to 93?:?7) with modest to good yields. The method has been applied to a variety of phenylallene derivatives as well as alkyl-substituted allenes. This journal is

Enantioselective Copper-Catalyzed Three-Component Carboboronation of Allenes: Access to Functionalized Dibenzo [b,f][1,4]oxazepine Derivatives

Deng, Hao,Meng, Ziwei,Wang, Sifan,Zhang, Zheming,Zhang, Yaqi,Shangguan, Yu,Yang, Fazhou,Yuan, Dekai,Guo, Hongchao,Zhang, Cheng

supporting information, p. 3582 - 3587 (2019/07/17)

A copper-catalyzed enantioselective three-component difunctionalization of allenes with seven-membered cyclic imines and bis(pinacolato)diboron (B2(Pin)2) to approach functionalized dibenzo[b,f][1,4]oxazepine derivatives is developed. The chiral products are obtained in up to 81% yield, >20:1 dr, and 98% ee when either a chiral diphosphine ligand or a chiral ferrocenyl-based P,N-ligand is used. Furthermore, the reaction exhibits reversed diastereoselectivities when the chiral diphosphine ligand and the chiral P,N-ligand are used respectively. (Figure presented.).

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