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3-Quinolineboronic acid

3-Quinolineboronic acid structure

3-Quinolineboronic acid 

structure
  • CAS No:

    191162-39-7

  • Formula:

    C9H8BNO2

  • Chemical Name:

    3-Quinolineboronic acid

  • Synonyms:

    CHEMBRDG-BB 4003837;3-QUINOLINEBORONIC ACID;3-QUINOLYL BORONIC ACID;3-QUINOLINYLBORONI ACID;3-QUINOLINYLBORONIC ACID;AKOS BRN-0151;RARECHEM AK VD 0023;QUINOLIN-3-YLBORONIC ACID

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

light pink or orange to light brown powder

3-Quinolineboronic acid Basic Attributes

172.98

173.064804

8764547

0

DTXSID60370433

29334900

Characteristics

53.4

-0.08540

Light pink or orange to light brown Powder

1.28±0.1 g/cm3(Predicted)

148-155°C

400.3±37.0 °C(Predicted)

195.9±26.5 °C

1.645

Keep Cold

0.066mmHg at 25°C

Safety Information

IRRITANT, KEEP COLD

NONH for all modes of transport

3

36/37/38-22

36/37/39-26-22-37-36

Xn,Xi

Irritant

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3-Quinolineboronic acid Use and Manufacturing

Methods of Manufacturing

General procedure: To a two-neck 250mL round bottom flask, triisopropyl borate (3.30mL, 29.06mmol) and 3-bromoquinoline (3.00g, 14.49mmol) was dissolved in dry THF (100mL), then n-butyllithium (14.50mL of a 2M solution in hexane, 29.00mmol) was added dropwise via a dropping funnel over 1h under NCompound 3-bromo-quinoline (3-bromoquinoline) 10g (48.06mmol) and triisopropylborate (triisopropylborate) 22mL (96.13mmol) dissolved in 200mL of THF and then, at -75 ° C n-BuLi 53mL (96.13mmol) of It was added slowly. After stirring at ° C or less for 20 minutes into the 2N HCl, it was adjusted to pH 7 neoteumyeonseo a 5NNaOH slowly. Ethyl acetate (Ethyl acetate) and was extracted with distilled water, methanol and recrystallization conducted by removing water to give the title compound21-45.95g (72percent).To a solution of compound 3-bromoquinoline (2.08 g, 10 mmol), triisopropyl borate (2.3g, 12 mmol) in THF (20 mL) was added n-BuLi (4 mL, 2.5 M in hexane) at -78PREPARATION 98

Uses

Reactant for: Preparation of P1-substituted symmetry-based human immunodeficiency virus protease inhibitors with antiviral activity against drug-resistant viruses Preparation of heterobiaryls via Suzuki-Miyaura cross-coupling with heteroaryl halides in co

Computed Properties

Molecular Weight:172.98
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:173.0648087
Monoisotopic Mass:173.0648087
Topological Polar Surface Area:53.4
Heavy Atom Count:13
Complexity:177
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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