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(2R*,4R*)-2,4-dichloropentane is a chiral organic compound with the molecular formula C5H10Cl2. It is a colorless liquid with a density of 1.1 g/cm3 and a boiling point of 180-181°C. (2R*,4R*)-2,4-dichloropentane is characterized by two chiral centers at the second and fourth carbon atoms, resulting in four stereoisomers. The specific (2R*,4R*) configuration indicates that the chlorine atoms are positioned on the right side of the molecule when viewed from the perspective of the highest priority group. (2R*,4R*)-2,4-dichloropentane is used as a synthetic intermediate in the production of various chemicals and pharmaceuticals, and it is also employed as a solvent in some industrial processes. Due to its potential environmental and health risks, proper handling and disposal are essential when working with (2R*,4R*)-2,4-dichloropentane.

1625-67-8

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1625-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1625-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1625-67:
(6*1)+(5*6)+(4*2)+(3*5)+(2*6)+(1*7)=78
78 % 10 = 8
So 1625-67-8 is a valid CAS Registry Number.

1625-67-8Upstream product

1625-67-8Downstream Products

1625-67-8Relevant academic research and scientific papers

Flexible molecules with defined shape XI[≠]. - Conformer equilibria in 2,4-disubstituted pentane derivatives

Hoffmann, Reinhard W.,Stenkamp, Dirk,Trieselmann, Thomas,G?ttlich, Richard

, p. 2915 - 2927 (1999)

2,4-Disubstituted penfanes are molecules which adopt essentially only two conformations. Substituents have been varied in order to find those which lead to a strong preference of the conformer equilibrium. Studying 2- substituted 4-methylpentanes 3 and 4-benzyloxypentanes 12, it has been shown that substituent effects on the conformer equilibria are not additive, as would be expected on the grounds of steric effects alone. Rather, interactions between polar groups reinforce the bias of the conformer equilibria. When applied to 2,4-disubstituted pentanes, substituents such as chloro or phthalimido shift the conformer equilibrium to the side of the gg conformer with preferences exceeding 90%.

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