619-45-4 | Methyl 4-aminobenzoate

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$8.00	$6.00
100g	98%	in stock	$21.00	$15.00
500g	98%	in stock	$105.00	$74.00

Description

• Catalog Number: AG64156
• Chemical Name: Methyl 4-aminobenzoate
• CAS Number: 619-45-4
• Molecular Formula: C8H9NO2
• Molecular Weight: 151.16256
• MDL Number: MFCD00007891
• SMILES: COC(=O)c1ccc(cc1)N
• NSC Number: 3783

Computed Properties

• Complexity: 139
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1.4

Literature

• Where's the charge? Protonation sites in gaseous ions change with hydration.

  Journal of the American Chemical Society 20120926

• Butamben derivatives enhance BMP-2-stimulated commitment of C2C12 cells into osteoblasts with induction of voltage-gated potassium channel expression.

  Bioorganic & medicinal chemistry letters 20111215

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Methyl 4-isonicotinamido-benzoate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20100801

• Cytotoxic metabolites from the wood-decayed fungus Xylaria sp. BCC 9653.

  Chemical & pharmaceutical bulletin 20071101

• Efficient preparation of nitrosoarenes for the synthesis of azobenzenes.

  The Journal of organic chemistry 20050318

• A new monoclinic polymorph of methyl p-aminobenzoate.

  Acta crystallographica. Section C, Crystal structure communications 20040101

• Purification and characterization of PrbA, a new esterase from Enterobacter cloacae hydrolyzing the esters of 4-hydroxybenzoic acid (parabens).

  The Journal of biological chemistry 20030411

• Total synthesis of the alkaloids martinelline and martinellic acid via a hetero Diels-Alder multicomponent coupling reaction.

  Organic letters 20020822

• Antagonism of chemotherapeutic activity of p-aminosalicylic acid in experimental tuberculosis by p-aminobenzoic acid.

  Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) 19531201