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72072-16-3

72072-16-3 Structure

72072-16-3 Structure
IdentificationBack Directory
[Name]

4-Butyl-2-methylaniline
[CAS]

72072-16-3
[Synonyms]

P-BUTYL-O-TOLUIDINE
4-BUTYL-2-METHYLANILINE
2-Methyl-4-butylaniline
4-N-BUTYL-2-METHYLANILINE
2-Methyl-4-n-butylaniline
4-butyl-2-methylbenzenamine
4-BUTYL-2-METHYLANILINE: TECH.
Benzenamine, 4-butyl-2-methyl-
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C11H17N
[MDL Number]

MFCD00190660
[MOL File]

72072-16-3.mol
[Molecular Weight]

163.26
Chemical PropertiesBack Directory
[Boiling point ]

264.3±9.0 °C(Predicted)
[density ]

0.939±0.06 g/cm3(Predicted)
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Oil
[pka]

4.75±0.10(Predicted)
[color ]

Red to Dark Brown
[InChI]

InChI=1S/C11H17N/c1-3-4-5-10-6-7-11(12)9(2)8-10/h6-8H,3-5,12H2,1-2H3
[InChIKey]

JTXOXRXZCAMPHL-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(CCCC)C=C1C
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-53
[Safety Statements ]

36/37
[WGK Germany ]

WGK 3
[HS Code ]

2921490090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

4-Butyl-2-methylaniline is used for the preparation of a number of substituted acetamides which are antagonists of MDR proteins for treatment of drug-resistant cancers.
[Biological Activity]

SMIP004-7 is a cell penetrantpotent and selective ubiquinone uncompetitive inhibitor of mitochondrial Complex I (NADH:ubiquinone oxidoreductase). SMIP004-7 selectively binds to a distinct N-terminal region of Complex I catalytic subunit NDUFS2which leads to rapid disassembly of Complex I. SMIP004-7 potently inhibits growth of triple-negative breast cancer xenografts in mice.
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