4-Chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]benzenepropanoic acid
Properties
- Molecular formula
- C14H18ClNO4
- Molar mass
- 299.75 g/mol
- Exact mass
- 299.0924 Da
- logP
- 3.58Crippen estimate
- Polar surface area
- 79.1 Ų
- H-bond donors / acceptors
- 2 / 3
- Rotatable bonds
- 4
Hazards
No GHS classification is on file for this compound. That is not evidence that it is harmless. Search the SDS library
Identifiers
CAS number
284493-65-8SMILES
CC(C)(C)OC(O)=NC(CC(=O)O)c1ccc(Cl)cc1InChIKey
ZPXVKCUGZBGIBW-UHFFFAOYSA-NInChI
InChI=1S/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)Weigh it out
Type any one amount. The others follow from the molar mass.
Names and synonyms
3 names
- Benzenepropanoic acid, 4-chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]-
- 3-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid
- 3-[[(tert-Butoxy)carbonyl]amino]-3-(4-chlorophenyl)propanoic acid
Work with 4-Chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]benzenepropanoic acid
Stereoisomers, salts and isotopologues
The same compound in another form: other stereochemistry, a salt or hydrate, the free acid or base, or an isotope-labelled version.
Similar compounds
(3S)-3-(((tert-Butoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid479064-88-577 % similar
(betaR)-beta-(((1,1-Dimethylethoxy)carbonyl)amino)-4-fluorobenzenepropanoic acid479064-94-377 % similar
(3S)-3-(((tert-Butoxy)carbonyl)amino)-3-(4-methylphenyl)propanoic acid479064-96-577 % similar
(3R)-3-(((tert-Butoxy)carbonyl)amino)-3-(4-methylphenyl)propanoic acid479064-97-677 % similar
β-[[(1,1-Dimethylethoxy)carbonyl]amino]benzenepropanoic acid14676-01-876 % similar
(βS)-4-Bromo-β-[[(1,1-dimethylethoxy)carbonyl]amino]benzenepropanoic acid261165-06-475 % similar
β-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-fluorobenzenepropanoic acid284493-59-071 % similar
(R)-3-((tert-Butoxycarbonyl)amino)-4-(4-chlorophenyl)butanoic acid218608-96-969 % similar
Tanimoto similarity of circular fingerprints over the whole catalogue. All similar compounds