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25629-50-9

3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride

CAS: 25629-50-9

Molecular Formula: C11H7Cl2NO2

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25629-50-9 - Names and Identifiers

Name 3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride
Synonyms Nsc 81237
CMIC Chloride
Einecs 247-137-4
3-(O-CHLOROPHENYL)-5-METHYL-4-CHLOROCARBONYLISOXAZOLE
3-(2-chlorophenyl)-5-methyl-4-isoxazolecarbonylchlorid
3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarbonyl chloride
3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride
3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarbonyl chloride
4-Isoxazolecarbonyl chloride, 3-(2-chlorophenyl)-5-methyl-
3-(2-Chlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl chloride
4-Isoxazolecarbonyl chloride, 3-(o-chlorophenyl)-5-methyl- (8ci)
CAS 25629-50-9
EINECS 247-137-4
InChI InChI=1/C11H7Cl2NO2/c1-6-9(11(13)15)10(14-16-6)7-4-2-3-5-8(7)12/h2-5H,1H3

25629-50-9 - Physico-chemical Properties

Molecular FormulaC11H7Cl2NO2
Molar Mass256.08
Density1.381±0.06 g/cm3(Predicted)
Melting Point41-42°C
Boling Point381.7±42.0 °C(Predicted)
Flash Point184.6°C
Water Solubility128.2mg/L at 25℃
Vapor Presure0.001Pa at 25℃
BRN791931
pKa-5.80±0.50(Predicted)
Storage Condition2-8℃
SensitiveMoisture Sensitive
Refractive Index1.574
MDLMFCD00020811
UseFor pharmaceutical intermediates

25629-50-9 - Risk and Safety

Risk Codes34 - Causes burns
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/45 -
UN IDs3261
TSCAYes
Hazard Class8
Packing GroupII

25629-50-9 - Reference Information

LogP2.61 at 25℃
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Uses Used as a pharmaceutical intermediate
An intermediate of chlorobenzazole penicillin sodium.
production method oxime with o-chlorobenzaldehyde and hydroxylamine hydrochloride under alkaline conditions to generate o-chlorobenzoxime, and then chlorinated with chlorine to obtain o-chlorobenzoxime chloride, and then combined with ethyl acetoacetate ring to hydrolyze the ester group to generate 3-(o-chlorophenyl)-5-methyl -4-isoxazole, finally, the product was prepared by chlorination of phosphorus pentachloride.
Last Update:2024-04-09 02:00:07
25629-50-9
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