CAS 101084-81-5

Acido (3-carbossi-5-nitrofenil)boronico

Formula: C₇H₆BNO₆

InChI: InChI=1/C7H6BNO6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3,12-13H,(H,10,11)

SMILES: c1c(cc(cc1B(O)O)N(=O)=O)C(=O)O

Sinonimi:

• 3-Borono-5-nitrobenzoic acid
• 3-(Dihydroxyboranyl)-5-Nitrobenzoic Acid
• 3-Carboxy-5-nitrophenylboronic acid

3-Carboxy-5-nitrophenylboronic Acid (contains varying amounts of Anhydride)

CAS: 101084-81-5

Formula: C₇H₆BNO₆

Purezza: 97.0 to 109.0 %

Colore e forma: White to Light yellow powder to crystal

Peso molecolare: 210.94

Ref: 3B-C2385

3-Carboxy-5-nitrobenzeneboronic acid, 97%

CAS: 101084-81-5

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₇H₆BNO₆

Purezza: 97%

Colore e forma: White to pale cream, Powder

Peso molecolare: 210.94

Ref: 02-H29348

Benzoic acid, 3-borono-5-nitro-

CAS: 101084-81-5

Formula: C₇H₆BNO₆

Purezza: 96%

Colore e forma: Solid

Peso molecolare: 210.9366

Ref: IN-DA0003P8

3-Carboxy-5-nitrophenylboronic acid

CAS: 101084-81-5

Formula: C₇H₆BNO₆

Peso molecolare: 210.94

Ref: 7W-GK0182

3-Carboxy-5-nitrophenylboronic acid

CAS: 101084-81-5

Purezza: 95%

Peso molecolare: 210.94

Ref: FT-C1332

3-Carboxy-5-nitrobenzeneboronic acid

CAS: 101084-81-5

3-Carboxy-5-nitrobenzeneboronic acid

Formula: C₇H₆BNO₆

Purezza: 98%

Colore e forma: Solid-Powder

Peso molecolare: 210.93663

Ref: 54-OR10400

3-Carboxy-5-nitrophenylboronic acid

CAS: 101084-81-5

3-Carboxy-5-nitrophenylboronic acid is a linker molecule that reacts with the active site of enzymes by reversible binding. It can be used in the design of micelles, which are spherical nanoparticles consisting of a hydrophilic shell and a hydrophobic core. 3-Carboxy-5-nitrophenylboronic acid has been shown to be an effective inhibitor of tumor growth by inhibiting cancer cell proliferation and inducing apoptosis. This compound was also shown to inhibit the growth of human colon tumor cells in culture. The ester linkages in this molecule are cleaved by water molecules, releasing nitro groups and generating reactive species that react with boronic acids to form covalent bonds. This process is called transesterification, which is an important reaction for making polymers.

Formula: C₇H₆BNO₆

Purezza: Min. 95%

Peso molecolare: 210.94 g/mol

Ref: 3D-FC37899

3-Carboxy-5-nitrophenylboronic acid

CAS: 101084-81-5

Formula: C₇H₆BNO₆

Purezza: 96%

Colore e forma: Solid

Peso molecolare: 210.94

Ref: 10-F016141