(1′R,3R)-(+)-1-(1′-Phenylethyl)-5-oxo-3-pyrrolidinecarboxylic acid

Modify Date: 2025-08-25 08:37:26

(1′R,3R)-(+)-1-(1′-Phenylethyl)-5-oxo-3-pyrrolidinecarboxylic acid Structure
(1′R,3R)-(+)-1-(1′-Phenylethyl)-5-oxo-3-pyrrolidinecarboxylic acid structure
Common Name (1′R,3R)-(+)-1-(1′-Phenylethyl)-5-oxo-3-pyrrolidinecarboxylic acid
CAS Number 99735-43-0 Molecular Weight 233.26300
Density 1.267g/cm3 Boiling Point 460.1ºC at 760 mmHg
Molecular Formula C13H15NO3 Melting Point 210-213ºC(lit.)
MSDS Chinese USA Flash Point 232.1ºC

 Names

Name 5-Oxo-1-(1-phenylethyl)pyrrolidine-3-carboxylic acid
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.267g/cm3
Boiling Point 460.1ºC at 760 mmHg
Melting Point 210-213ºC(lit.)
Molecular Formula C13H15NO3
Molecular Weight 233.26300
Flash Point 232.1ºC
Exact Mass 233.10500
PSA 57.61000
LogP 1.61860
InChIKey CFGKWSDAMXTRHE-MWLCHTKSSA-N
SMILES CC(c1ccccc1)N1CC(C(=O)O)CC1=O

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases S24/25
RIDADR NONH for all modes of transport
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Bioassay

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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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 Synonyms

(1'r, 3r)-1-(1'-phenylethyl)-5-oxo-3-pyrrolidine carboxylic acid
MFCD03093924
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