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460720-14-3

460720-14-3 Structure

460720-14-3 Structure
IdentificationBack Directory
[Name]

(αS)-Cyclohexanebutanoic Acid α-[[(1S)-1-Carboxyethyl]aMino] cyclohexanebutanoic Acid α-Ethyl Ester
[CAS]

460720-14-3
[Synonyms]

Delapril Impurity 8
Enalapril Maleate IMpurity-G
Enalapril maleate EP Impurity G
Enalapril Cyclohexyl ECPPA Analog
(2S)-2-[[(2S)-4-cyclohexyl-1-ethoxy-1-oxobutan-2-yl]amino]propanoic acid
Cyclohexanebutanoic acid, α-[[(1S)-1-carboxyethyl]amino]-, α-ethyl ester, (αS)- (9CI)
(αS)-Cyclohexanebutanoic Acid α-[[(1S)-1-Carboxyethyl]amino] cyclohexanebutanoic Acid α-Ethyl Ester
(αS)-Cyclohexanebutanoic Acid α-[[(1S)-1-Carboxyethyl]aMino] cyclohexanebutanoic Acid α-Ethyl Ester
Trandolapril ECPP alanine saturated analogue (Enalapril EP Impurity G/ Enalapril Cyclohexyl ECPPA Analog)
Enalapril EP Impurity G/ Enalapril Cyclohexyl ECPPA Analog (Trandolapril ECPP alanine saturated analogue)
[Molecular Formula]

C15H27NO4
[MDL Number]

MFCD30719917
[MOL File]

460720-14-3.mol
[Molecular Weight]

285.38
Chemical PropertiesBack Directory
[Melting point ]

>152°C (dec.)
[Boiling point ]

412.1±30.0 °C(Predicted)
[density ]

1.067±0.06 g/cm3(Predicted)
[storage temp. ]

Refrigerator
[solubility ]

Ethanol (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

2.15±0.10(Predicted)
[color ]

White
[InChI]

1S/C15H27NO4/c1-3-20-15(19)13(16-11(2)14(17)18)10-9-12-7-5-4-6-8-12/h11-13,16H,3-10H2,1-2H3,(H,17,18)/t11-,13-/m0/s1
[InChIKey]

SSKKXRIKYHEFTJ-AAEUAGOBSA-N
[SMILES]

[N+H2]([C@@H](CCC1CCCCC1)C(=O)OCC)[C@@H](C)C(=O)[O-]
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H335-H315-H319
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

(αS)-Cyclohexanebutanoic Acid α-[[(1S)-1-Carboxyethyl]amino]cyclohexanebutanoic acid α-ethyl ester is an impurity of Enalaprilat maleate.
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