CAS No.127972-00-3 | 2-Methoxy-5-methylphenylboronic acid
Name:2-Methoxy-5-methylphenylboronic acid CAS No.127972-00-3 MF:C8H11BO3 MW:165.98 Purity:97% Package: 5g,25g,100g,500g,1kg,25kg Worldwide Delivery
Categories：
Analytical Chemicals
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Product introduction
Introduction and application of CAS No.127972-00-3 | 2-Methoxy-5-methylphenylboronic acid
2-Methoxy-5-methylphenylboronicacid is a boronate ester that can be used for the organic synthesis of diverse substituted aryl compounds. It has been used to synthesize the allylamine group in a stereoselective manner, which is an important process for the production of pharmaceuticals.
2-Methoxy-5-methylphenylboronicacid has also been used in cross-coupling reactions with chloride and histidine, as well as trisubstituted chlorides. This compound also has the ability to produce amines by irradiation or by heating in the presence of amines or aminium salts.
Synonyms:
5-Methyl-2-methoxyphenylboronicacid;
(2-methoxy-5-methylphenyl)boronicacid(SALTDATA:FREE);
2-Methoxy-5-Methylphenyl boronic Acid (contains varyinga Mounts of Anhydride);
BORONICACID,(2-METHOXY-5-METHYLPHENYL)-(9CI);
2-Methoxy-5-methylphenyl boronic acid>=95%;
5-METHOXY-2-METHYLPHENYLBORONICACID
Specification of CAS No.127972-00-3 | 2-Methoxy-5-methylphenylboronic acid
|
ITEMS |
SPECIFICATION |
|
CAS No. |
127972-00-3 |
|
MF |
C8H11BO3 |
|
MW |
165.98 |
|
Melting point |
92-97 °C (lit.) |
|
Boiling point |
342.0±52.0 °C(Predicted) |
|
Density |
1.14±0.1 g/cm3(Predicted) |
|
acidity coefficient(pKa) |
8.65±0.58(Predicted) |
Package of CAS No.127972-00-3 | 2-Methoxy-5-methylphenylboronic acid
Package:100g; 500g; 1kg; 25kg;bulk package
Transportation: by courier/ by air/ by sea
Related Articles of CAS No.127972-00-3 | 2-Methoxy-5-methylphenylboronic acid
Stereoselective synthesis of (E)-3, 3-diaryl and (E)-3-aryl-3-aryloxy allylamines and allylalcohols from trans-cinnamyl chloride and alcohol
J Limberger, TS Claudino, AL Monteiro - RSC advances, 2014 - pubs.rsc.org
… The optimisation was carried out at room temperature for one hour using substrate 5a and
2-methoxy-5-methylphenylboronic acid as coupling partners (Table 1). Initially, a phosphine-…
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