(6-Methoxybenzo[b]thiophen-2-yl)boronic acid

Base Information

• Chemical Name: (6-Methoxybenzo[b]thiophen-2-yl)boronic acid
• CAS No.: 182133-35-3
• Molecular Formula: C9H9BO3S
• Molecular Weight: 208.046
• Hs Code.: 2934999090
• European Community (EC) Number: 879-225-9
• DSSTox Substance ID: DTXSID40441736
• Wikidata: Q82258653
• Mol file: 182133-35-3.mol

Synonyms:182133-35-3;(6-Methoxybenzo[b]thiophen-2-yl)boronic acid;6-METHOXYBENZO[B]THIOPHENE-2-BORONIC ACID;(6-Methoxy-1-benzothiophen-2-yl)boronic acid;6-methoxybenzo[b]thiophen-2-ylboronic acid;SCHEMBL225978;DTXSID40441736;PNRDOYJXKKKYSU-UHFFFAOYSA-N;MFCD09952075;AKOS015950239;SB67111;PS-13008;6-methoxy-benzo[b]thiophen-2-boronic acid;6-methoxy-benzo[b]thiophene-2-boronic acid;6-methoxybenzo[b] thiophene-2-boronic acid;(6-Methoxybenzo[b]thiophen-2-yl)boronicacid;CS-0357297;FT-0751254;[6-(Methyloxy)-1-benzothien-2-yl]boronic acid;EN300-4266722;A926076;J-518853;Z1269238917

Chemical Property of (6-Methoxybenzo[b]thiophen-2-yl)boronic acid

Chemical Property:

• Boiling Point: 423.068 °C at 760 mmHg
• Flash Point: 209.664 °C
• PSA: 77.93000
• Density: 1.354 g/cm³
• LogP: 0.58970
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 208.0365455
• Heavy Atom Count: 14
• Complexity: 203

Purity/Quality:

97% ^*data from raw suppliers

(6-?Methoxybenzo[b]?thiophen-?2-?yl)?boronicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B(C1=CC2=C(S1)C=C(C=C2)OC)(O)O
• Uses: (6-?Methoxybenzo[b]?thiophen-?2-?yl)?boronic Acid is used as a reactant in the synthetic preparation of diaminobenzo[b]thiophenes as active site directed thrombin inhibitors and anticoagulants.

Technology Process of (6-Methoxybenzo[b]thiophen-2-yl)boronic acid

There total 7 articles about (6-Methoxybenzo[b]thiophen-2-yl)boronic acid 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: 99.0%

→ 6-methoxy-benzo[b]thiophen-2-yl boronic acid (182133-35-3)

Guidance literature:

Reference yield: 71.0%

6-methoxy-benzo[b]thiophene (90560-10-4) → 6-methoxy-benzo[b]thiophen-2-yl boronic acid (182133-35-3)

Guidance literature:

With n-butyllithium; Triisopropyl borate; In tetrahydrofuran; hexane; at -60 ℃; for 0.5h;

Reference yield: 71.0%

C15H21BO3S → 6-methoxy-benzo[b]thiophen-2-yl boronic acid (182133-35-3)

Guidance literature:

With hydrogenchloride; In ethyl acetate;

DOI:10.1021/jm9903388

upstream raw materials:

6-methoxy-benzo[b]thiophene

3-methoxybenzenethiol

Triisopropyl borate

Downstream raw materials:

6-methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophene

2-phenyl-6-methoxybenzothiophene

2-(4'-methoxyphenyl)-6-methoxybenzothiophene

6-methoxy-2-(p-tolyl)benzo[b]thiophene

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