7149-10-2 | 4-Hydroxy-3-methoxybenzylamine, HCl

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$15.00	$10.00
10g	98%	in stock	$18.00	$12.00
25g	98%	in stock	$28.00	$19.00
100g	98%	in stock	$86.00	$60.00
500g	98%	in stock	$203.00	$142.00

Description

• Catalog Number: AB67629
• Chemical Name: 4-Hydroxy-3-methoxybenzylamine, HCl
• CAS Number: 7149-10-2
• Molecular Formula: C8H12ClNO2
• Molecular Weight: 189.63938
• MDL Number: MFCD00012864
• SMILES: COc1cc(CN)ccc1O.Cl
• NSC Number: 62020

Computed Properties

• Complexity: 119
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Literature

• Functional validation of Capsicum frutescens aminotransferase gene involved in vanillylamine biosynthesis using Agrobacterium mediated genetic transformation studies in Nicotiana tabacum and Capsicum frutescens calli cultures.

  Plant science : an international journal of experimental plant biology 20121001

• Synthesis of stable isotope-labeled precursors for the biosyntheses of capsaicinoids, capsinoids, and capsiconinoids.

  Bioscience, biotechnology, and biochemistry 20110101

• Functional loss of pAMT results in biosynthesis of capsinoids, capsaicinoid analogs, in Capsicum annuum cv. CH-19 Sweet.

  The Plant journal : for cell and molecular biology 20090901

• Valine pathway is more crucial than phenyl propanoid pathway in regulating capsaicin biosynthesis in Capsicum frutescens mill.

  Journal of agricultural and food chemistry 20060906

• Utilization of capsaicin and vanillylamine as growth substrates by Capsicum (hot pepper)-associated bacteria.

  Environmental microbiology 20060301