| Identification | More | [Name]
4'-Chloroacetoacetanilide | [CAS]
101-92-8 | [Synonyms]
4'-CHLOROACETACETANILIDE
4'-CHLOROACETOACETANILIDE
AAPCA
ACETOACET-P-CHLORANILIDE
ACETOACET-P-CHLOROANILIDE
LABOTEST-BB LT01274571
N-(4-CHLOROPHENYL)-3-OXOBUTANAMIDE
N-ACETOACETYL-4-CHLOROANILINE
P-CHLOROACETOACETANILIDE
TIMTEC-BB SBB003431
4’-chloro-acetoacetanilid
Acetoacetanilide, 4'-chloro-
Acetoacetanilide, p-chloro-
Acetoacetic acid-4-chloroanilide
Acetoacetyl-4-chloroanilide
Butanamide, 3-oxo-N-(4-chlorophenyl)-
n-(4-chlorophenyl)-3-oxo-butanamid
N-(4-Chloro-phenyl)-3-oxo-butyramide
N-(4-Chlorophenyl)acetoacetamide
p-chloro-acetoacetanilid | [EINECS(EC#)]
202-989-6 | [Molecular Formula]
C10H10ClNO2 | [MDL Number]
MFCD00000613 | [Molecular Weight]
211.64 | [MOL File]
101-92-8.mol |
| Hazard Information | Back Directory | [Chemical Properties]
off-white to beige crystalline powder | [Uses]
4′-Chloroacetoacetanilide was used in recombinant androgen receptor competitive binding assay for analysis of natural, synthetic and environmental chemicals. | [Definition]
ChEBI:P-Chloroacetoacetanilide is an anilide. | [General Description]
4′-Chloroacetoacetanilide was trilithiated with lithium diisopropylamide and condensed with several aromatic esters, followed by neutralization, separate acid cyclization and rearrangements to yield 4-anilino-6-aryl-2H-pyran-2-ones. It undergoes three-component reaction with a mixture of aromatic aldehyde and 5-aminotetrazole to form N,7-diaryl-5-methyl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxamide. | [Safety Profile]
Moderately toxic by intraperitonealroute. Combustible whenexposed to heat or flame. Dangerous: see ANILINE andCYANIDE. Can react vigorously with oxidizing materials.To fight fire, use water, foam, CO2, water mist, drychemical. When heated to decompo |
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