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3,3-dibromopentane is an organic compound with the chemical formula C5H10Br2. It is a colorless liquid at room temperature and is derived from pentane, a five-carbon alkane, with two bromine atoms attached to the third carbon atom. This symmetrical dibromide is used as a chemical intermediate in the synthesis of various organic compounds, such as pharmaceuticals and agrochemicals. Due to its reactivity, 3,3-dibromopentane can undergo substitution, elimination, and addition reactions, making it a versatile building block in organic chemistry. It is also known for its potential use as a flame retardant and as a solvent in certain industrial applications. However, like many halogenated hydrocarbons, 3,3-dibromopentane may have environmental and health concerns, and its use is subject to regulatory controls.

54653-27-9

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54653-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54653-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,5 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54653-27:
(7*5)+(6*4)+(5*6)+(4*5)+(3*3)+(2*2)+(1*7)=129
129 % 10 = 9
So 54653-27-9 is a valid CAS Registry Number.

54653-27-9Upstream product

54653-27-9Downstream Products

54653-27-9Relevant academic research and scientific papers

Induced Fitting and Polarization of a Bromine Molecule in an Electrophilic Inorganic Molecular Cavity and Its Bromination Reactivity

Hayashi, Yoshihito,Inada, Yasuhiro,Katayama, Misaki,Kikukawa, Yuji,Kitajima, Hiromasa,Seto, Kensuke,Watanabe, Daiki,Yamashita, Shohei

supporting information, p. 14399 - 14403 (2020/07/13)

Dodecavanadate, [V12O32]4? (V12), possesses a 4.4 ? cavity entrance, and the cavity shows unique electrophilicity. Owing to the high polarizability, Br2 was inserted into V12, inducing the inversion of one of the VO5 square pyramids to form [V12O32(Br2)]4? (V12(Br2)). The inserted Br2 molecule was polarized and showed a peak at 185 cm?1 in the IR spectrum. The reaction of V12(Br2) and toluene yielded bromination of toluene at the ring, showing the electrophilicity of the inserted Br2 molecule. Compound V12(Br2) also reacted with propane, n-butane, and n-pentane to give brominated alkanes. Bromination with V12(Br2) showed high selectivity for 3-bromopentane (64 %) among the monobromopentane products and preferred threo isomer among 2-,3-dibromobutane and 2,3-dibromopenane. The unique inorganic cavity traps Br2 leading the polarization of the diatomic molecule. Owing to its new reaction field, the trapped Br2 shows selective functionalization of alkanes.

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