structure of 1072944-81-0

Ethyl 8-Bromo-4-Hydroxy-6-(Trifluoromethoxy)Quinoline-3-Carboxylate(CAS 1072944-81-0)

CAS No.: 1072944-81-0 Brand: MolBest
M. Ft.: C13H9BrF3NO4 Cat. No: G6846660
M. Wt.: 380.11 MDL: No record
Storage: 2-8°C Use: For laboratory research use only
HS CODE: 2933499090
Purity Grade Package Stock Price Quantity
98%
Documents:COASDS
RG 100MG In Stock 50 USD
98%
Documents:COASDS
RG 250MG In Stock 96 USD
98%
Documents:COASDS
RG 1G In Stock 283 USD
98%
Documents:COASDS
RG 5G In Stock 1187 USD
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Physical and chemical properties of 1072944-81-0

Boiling Point

379.7±37.0 °C at 760 mmHg

Density

1.7±0.1 g/cm3

Exact Mass

378.966705

Flash Point

183.4±26.5 °C

H Bond Acceptors

4

H Bond Donors

1

Index of Refraction

1.580

LogP

5.15

Molecular Formula

C13H9BrF3NO4

Molecular Weight

380.114

PSA

68.65000

Storage condition

2-8°C

Vapour Pressure

0.0±0.9 mmHg at 25°C

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Hazard Statements

H302 Harmful if swallowed
H315 Causes skin irritation
H319 Causes serious eye irritation
H335 May cause respiratory irritation

Safety Data Sheet

Q&A for CAS 1072944-81-0

1. How can I verify product quality?
Every batch is tested in accordance with ISO 9001 requirements. We provide a Certificate of Analysis (COA), NMR spectrum, purity report, and test methods with each shipment. Third-party retesting is supported, and we offer a full refund if our data is incorrect.

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Hazardous products are labeled and packaged in compliance with international regulations and shipped with an up-to-date Safety Data Sheet (SDS) to ensure safe and compliant transport.

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Applications of 1072944-81-0

Ethyl 8-bromo-4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate has several applications in research and industry:

  • Chemical Synthesis: It serves as an important intermediate in the synthesis of other bioactive compounds and pharmaceuticals.
  • Material Science: Its unique properties may be exploited in developing new materials with specific functionalities.
  • Biological Research: The compound is used in studies investigating quinoline derivatives' biological activities, contributing to drug discovery efforts.

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