Butanamide,N-(5-chloro-2-methylphenyl)-3-oxo

Modify Date: 2025-08-21 20:00:00

Butanamide,N-(5-chloro-2-methylphenyl)-3-oxo Structure
Butanamide,N-(5-chloro-2-methylphenyl)-3-oxo structure
Common Name Butanamide,N-(5-chloro-2-methylphenyl)-3-oxo
CAS Number 25233-50-5 Molecular Weight 225.67100
Density 1.247g/cm3 Boiling Point 386.1ºC at 760mmHg
Molecular Formula C11H12ClNO2 Melting Point N/A
MSDS N/A Flash Point 187.3ºC

 Names

Name N-(5-chloro-2-methylphenyl)-3-oxobutanamide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.247g/cm3
Boiling Point 386.1ºC at 760mmHg
Molecular Formula C11H12ClNO2
Molecular Weight 225.67100
Flash Point 187.3ºC
Exact Mass 225.05600
PSA 46.17000
LogP 2.63900
Vapour Pressure 3.62E-06mmHg at 25°C
Index of Refraction 1.572
InChIKey SGUFPRJAMBWKAZ-UHFFFAOYSA-N
SMILES CC(=O)CC(=O)Nc1cc(Cl)ccc1C

 Safety Information

HS Code 2924299090

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Bioassay

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Name: Cell-based high throughput primary assay to identify activators of GPR151
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id: GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
Name: AlphaScreen-based biochemical high throughput primary assay to identify activators of...
Source: The Scripps Research Institute Molecular Screening Center
Target: N/A
External Id: FBW7_ACT_ALPHA_1536_1X%ACT PRUN
Name: AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
Source: The Scripps Research Institute Molecular Screening Center
External Id: MITF_INH_Alpha_1536_1X%INH PRUN
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 Synonyms

Acetoacet-5-chloro-2-toluidide
Acetessigsaeure-(5-chlor-2-methyl-anilid)
1-acetoacetylamino-2-methyl-5-chlorobenzene
Acetoacet-5-chlor-o-toluidid
N-(5-Chloro-2-methyl-phenyl)-3-oxo-butyramide
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