Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate)

Base Information

• Chemical Name: Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate)
• CAS No.: 1236031-63-2
• Molecular Formula: C₉H₈BNO₂*ClH
• Molecular Weight: 209.44
• Hs Code.: 2933499090
• Mol file: 1236031-63-2.mol

Synonyms:Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate)

Chemical Property of Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate)

Chemical Property:

• PSA: 53.35000
• LogP: 0.71660

Purity/Quality:

97% ^*data from raw suppliers

Isoquinolin-6-ylboronicacidhydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T
• Statements: 25-41
• Safety Statements: 26-39-45

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Isoquinolin-6-ylboronic acid, HCl

Technology Process of Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate)

There total 3 articles about Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

hydrogenchloride (7647-01-0,15364-23-5) + 6-bromo-isoquinoline (34784-05-9) + Triisopropyl borate (5419-55-6) → isoquinolin-6-ylboronic acid hydrochloride (1236031-63-2)

Guidance literature:

6-bromo-isoquinoline; Triisopropyl borate; With n-butyllithium; In tetrahydrofuran; at -78 - -20 ℃; for 2h;

hydrogenchloride; In tetrahydrofuran; water;

DOI:10.1002/chem.202104617

Reference yield: 49.0%

6-bromo-isoquinoline (34784-05-9) + Triisopropyl borate (5419-55-6) → isoquinolin-6-ylboronic acid hydrochloride (1236031-63-2)

Guidance literature:

6-bromo-isoquinoline; Triisopropyl borate; With n-butyllithium; In tetrahydrofuran; hexane; at -70 - 20 ℃; for 1h;

With hydrogenchloride; In tetrahydrofuran; hexane; water; at 20 ℃; for 1h;

Reference yield:

C15H20BNO2 → isoquinolin-6-ylboronic acid hydrochloride (1236031-63-2)

Guidance literature:

With hydrogenchloride; In tetrahydrofuran; water; at -20 ℃;

upstream raw materials:

6-bromo-isoquinoline

Triisopropyl borate

hydrogenchloride

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