Research chemical
CAS Number: 103772-14-1
Product details
For laboratory research and professional procurement workflows.
PubChem CID
13910947
Exact Mass
298.056527
InChIKey
CQPUZLMNORVQPG-UHFFFAOYSA-N
IUPAC Name
5-amino-1-cyclopropyl-6,7,8-trifluoro-4-oxoquinoline-3-carboxylic acid
SMILES String
Nc1c(F)c(F)c(F)c2c1c(=O)c(C(=O)O)cn2C1CC1
Appearance
5-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid is identified by CAS 103772-14-1, with molecular formula C13H9F3N2O3, molecular weight 298.22, InChIKey CQPUZLMNORVQPG-UHFFFAOYSA-N.
Yes. Submit an RFQ and specify COA requirements. Lot-specific COA depends on supplier confirmation.
Yes. Supplier SDS can be requested through the RFQ workflow before handling, storage, shipment, or procurement decisions.
Availability, pack size, lead time, and pricing are confirmed through RFQ.
Submit the CAS number, quantity, purity requirement, and destination country for sourcing review.
white to off-white powder
Physical State
solid
Melting Point
250.0 °C
Boiling Point
450.0 °C
Density
1.66 g/cm³
Water Solubility
slightly soluble
Flash Point
269.4 °C
Autoignition Temp
500.0 °C
Properties are provided as catalog reference data and may be confirmed through supplier documentation when required.
Heavy atom count
21
H-bond acceptors
5
H-bond donors
3
Rotatable bonds
2
Ring count
3
Aromatic rings
2
Topological polar surface area
85.32 Ų
Computed LogP
2.03
Fragment-like structure rule
Yes
Lead-like structure rule
Yes
Drug-like structure rule
Yes
Structure family
n heterocycle ligand
Precious metal motif
No
Transition metal motif
No
Phosphine ligand motif
No
N-heterocycle motif
Yes
Boronic acid motif
No
Computed structure descriptors generated from molecular structure. These are not experimental physical property values, supplier specifications, SDS data, or bioactivity claims.
Structural features
5-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (CAS 103772-14-1) is a quinoline derivative featuring a cyclopropyl group, an amino substituent, and trifluoro groups on the quinoline ring, along with a carboxylic acid moiety.
Sourcing context
Catalog reference for RFQ preparation, supplier confirmation, and research chemical sourcing review.
Research use context
For research use only. This compound serves as a valuable chemical intermediate in organic synthesis, especially for developing quinolone derivatives.
Documentation needs
Handle with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes.
Safety and handling reference content is available through documentation requests.
For supplier-issued SDS, request documentation before handling, storage, shipment, or procurement decisions.
Availability and lead time review: Confirmed by RFQ
Shipment documentation review: By request
For supplier-issued documentation by request, use the RFQ actions on this page.
DSL: pending; AICS: pending; ENCS: pending; ICSR: pending; TSCA: pending; IECSC: pending; INSQR: pending; REACH: pending; K-REACH: pending; SEA_Regulatory: pending
Registration values are catalog reference status cues and may require jurisdiction-specific review.