2,3-dichlorophenol

2,3-dichlorophenol structural formula

structural formula

business number 05v5
molecular formula c6h4cl2o
molecular weight 163
label

2,3-dichlorophenol,

dichlorophenol,

2,3-dichlorophenol,

2,3-dichloro-pheno,

medicine

numbering system

cas number:576-24-9

mdl number:mfcd00002160

einecs number:209-399-8

rtecs number:sk8450000

brn number:2043615

pubchem id:none

physical property data

1. physical property data

1. appearance: white crystal

2. melting point: 58℃

3. solubility: soluble in ether and chloroform and hot ethanol, difficult to dissolve in water and benzene

4. boiling point (ºc): 206

5. gas phase standard claims heat (enthalpy) (kj·mol-1 ):-168.0

toxicological data

none yet

ecological data

none yet

molecular structure data

5. molecular property data:

1. molar refractive index: 37.92

2. molar volume (cm3/mol): 111.7

3. isotonic specific volume (90.2k): 294.0

4. surface tension (dyne/cm): 47.8

5. polarizability (10-24cm3): 15.03

compute chemical data

1. reference value for hydrophobic parameter calculation (xlogp): none

2. number of hydrogen bond donors: 1

3. number of hydrogen bond acceptors: 1

4. number of rotatable chemical bonds: 0

5. number of tautomers: 3

6. topological molecule polar surface area 20.2

7. number of heavy atoms: 9

8. surface charge: 0

9. complexity: 97.1

10. number of isotope atoms: 0

11. determine the number of atomic stereocenters: 0

12. uncertain number of atomic stereocenters: 0

13. determine the number of chemical bond stereocenters: 0

14. number of uncertain chemical bond stereocenters: 0

15. number of covalent bond units: 1

properties and stability

1. properties: white crystal.

storage method

none yet

synthesis method

2. preparation method:

sulfonation of 1,2,3-trichlorobenzene into salt and high-pressure hydrolysis to obtain 3,4-dichloro-

2-hydroxybenzenesulfonic acid is obtained by hydrolysis with sulfuric acid to remove the sulfonic acid group.

purpose

3. usage:

as an organic synthesis intermediate. used in the synthesis of the drug diuretic acid.

resource:allhdi.com

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/30898

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