Grundinformationen
- Standard-SMILES
O=C(O)[C@@H]1CC[C@H](C(=O)O)C1- InChIKey
LNGJOYPCXLOTKL-SYDPRGILSA-N- Summenformel
- C7H10O4
- Durchschnittliche Molmasse
- 158,15 g/mol
- Monoisotopische Masse
- 158,0579088
Namen und Bezeichner
- Bevorzugter Name
- cis-1,3-Cyclopentanedicarboxylic acid
- IUPAC
- cis-(1R,3S)-cyclopentane-1,3-dicarboxylic acid
- Englischer Name
- (1S,3R)-cyclopentane-1,3-dicarboxylic acid
- Summenformel
- C7H10O4
- Molmasse
- 158.15
Namen und Synonyme
cis-1,3-Cyclopentanedicarboxylic acidRefChem:126383876-05-1(1R,3S)-Cyclopentane-1,3-dicarboxylic acidcis-cyclopentane-1,3-dicarboxylic acid(1S,3R)-cyclopentane-1,3-dicarboxylic acidrel-(1R,3S)-1,3-Cyclopentanedicarboxylic acidMFCD01311175cis-Norcamphoric acidrel-(1R,3S)-cyclopentane-1,3-dicarboxylic acid1,3-Cyclopentanedicarboxylic acid, cis-SCHEMBL1286869
Weitere Namen anzeigen
cis-1,3-Dicarboxycyclopentane1,3-Cyclopentanedicarboxylic acid, (1R,3S)-rel-cis-cyclopentane-1,3-dicarboxylic acid - [C87676]
DTXSID40285571LNGJOYPCXLOTKL-SYDPRGILSA-NAAA87605NSC42324NSC45402NSC-42324NSC-45402ZB1687
Datenbank-Bezeichner
- CAS
876-05-1- PubChem CID
- 238129
- DTXSID
DTXSID40285571- Nikkaji
- J79.997A
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,1
- Polarare Oberfläche (TPSA)
- 74,6 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 11
- Formalladung
- 0
- Komplexität
- 167
Physikochemische Eigenschaften
- Schmelzpunkt
- 121 °C · 121°C
- Siedepunkt
- 243.22 °C · 243.22°C (rough estimate)
- Dichte
- 1.2605 · 1.2605 (rough estimate)
- Brechungsindex
- 1.64 · 1.6400 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- Löslichkeit
- Chloroform (Slightly, Heated), Water (Slightly)
- Aggregatzustand
- Solid
- pka
- 1 · pK1:4.26;pK2:5.51 (25°C)
- Farbe
- Off-White to Pale Yellow
Sicherheit und Regulatorisches
Sicherheitsdaten
- hs_code
- 2917200090
Chemie und Industrie
Anwendungen
Verwenden(1R,3S)-Cyclopentane-1,3-dicarboxylic Acid is used in preparation of bis(Amino Acid) derivatives as inhibitors of human immunodeficiency virus replication and use for treatment of HIV infection.
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