113928-90-8

Basic information

• Product Name: Benzenemethanol, 3-amino-4-methoxy-
• Synonyms: Benzenemethanol, 3-amino-4-methoxy-;(3-AMino-4-Methoxyphenyl)Methanol
• CAS NO: 113928-90-8
• Molecular Formula: C₈H₁₁NO₂
• Molecular Weight: 153.18
• Mol File: 113928-90-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 95 °C(Solv: benzene (71-43-2))
• Boiling Point: 318.0±27.0 °C(Predicted)
• Appearance: /
• Density: 1.182±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 14.32±0.10(Predicted)
• CAS DataBase Reference: Benzenemethanol, 3-amino-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3-amino-4-methoxy-(113928-90-8)
• EPA Substance Registry System: Benzenemethanol, 3-amino-4-methoxy-(113928-90-8)

Safety Data

• Hazardous Substances Data: 113928-90-8(Hazardous Substances Data)

Usage

General Description

Benzenemethanol, 3-amino-4-methoxy- is a chemical compound that is classified as an amino alcohol. It features a benzene ring with a hydroxyl group attached, and a methoxy and amino group in the para positions. Benzenemethanol, 3-amino-4-methoxy- is commonly used in the production of pharmaceuticals and dyes due to its aromatic and nucleophilic properties. It is also known for its ability to act as a precursor in the synthesis of various organic compounds, and its potential application in the field of chemical research. Additionally, Benzenemethanol, 3-amino-4-methoxy- is recognized for its potential biological activity, making it a subject of interest in the development of new drugs and biochemical studies.

Upstream product

• 2840-26-8 3-amino-4-methoxybenzoic acid 
• 6378-19-4 4-methoxy-3-nitrobenzyl chloride 
• 31680-08-7 4-methoxy-3-nitrobenzaldehyde 
• 41870-24-0 (4-methoxy-3-nitrophenyl)methanol 
• 351003-10-6 3-amino-4-methoxy-benzaldehyde 
• 24812-90-6 methyl 3-amino-4-methoxybenzoate 

Relevant articles and documents

A solid-phase affinity labeling method for target-selective isolation and modification of proteins

Solid-phase affinity labeling of a target protein, peanut agglutinin (PNA), with the specifically designed chemical tool 1 selectively and effectively furnished the labeled PNA. Furthermore, this method was applicable to native human carbonic anhydrase II in red blood cell lysate using the chemical tool 2 without the need for tedious manipulations. This journal is

BIPHENYL-4-YL-SULFONIC ACID ARYLAMIDES AND THEIR USE AS THERAPEUTIC AGENTS

The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl sulfonamides and related compounds (collectively referred to herein as "BPSAAA compounds"), as described herein, and including, for example, biphenyl-4-sulfonic acid (hydroxyalkyl-phenyl)-amides and related compounds. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, in treatment and/or prevention, for example, of inflammation and/or joint destruction and/or bone loss; of disorders mediated by excessive and/or inappropriate and/or prolonged activation of the immune system; of, inflammatory and autoimmune disorders, for example, rheumatoid arthritis, psoriasis, psoriatic arthritis, chronic obstructive pulmonary disease (COPD), atherosclerosis, inflammatory bowel disease, ankylosing spondylitis, and the like; of disorders associated with bone loss, such as bone loss associated with excessive osteoclast activation in rheumatoid arthritis, osteoporosis, cancer associated bone disease, Paget's disease and the like.