40896-62-6

Basic information

• Product Name: [3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl)
• Synonyms: [3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl);(3-(Aminomethyl)phenyl)methanol hydrochloride
• CAS NO: 40896-62-6
• Molecular Formula: C₈H₁₁NO*ClH
• Molecular Weight: 173.63998
• Mol File: 40896-62-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: [3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: [3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl)(40896-62-6)
• EPA Substance Registry System: [3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl)(40896-62-6)

Safety Data

• Statements: 41
• Safety Statements: 26-39
• Hazardous Substances Data: 40896-62-6(Hazardous Substances Data)

Usage

Description

[3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl) is a white crystalline powder with the molecular formula C8H11NO.HCl. It is a chemical compound commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical intermediates. The hydrochloride salt form enhances its stability and solubility in water, making it easier to handle and work with in laboratory settings. However, it is important to handle this compound with care, as it can be harmful if ingested, inhaled, or comes into contact with skin.

Uses

Used in Pharmaceutical Industry:
[3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl) is used as a building block for the synthesis of various drugs and pharmaceutical intermediates. Its versatility in chemical reactions and stability in the hydrochloride salt form make it a valuable component in the development of new medications.
Used in Organic Chemistry:
[3-(aMinoMethyl)phenyl]Methanol hydrochloride (SALTDATA: HCl) is also used as a reagent in organic chemistry reactions. Its unique structure and properties allow it to participate in a variety of chemical processes, contributing to the synthesis of complex organic compounds.

Upstream product

• 874-97-5 3-(hydroxymethyl)benzonitrile 
• 226070-69-5 1,1-dimethylethyl {[3-(hydroxymethyl)phenyl]methyl}carbamate 

Downstream Products

• 743461-27-0 biphenyl-2-ylcarbamic Acid 1-{2-[3-(3-Hydroxymethylbenzyl)ureido]ethyl}piperidin-4-yl Ester 
• 1361952-84-2 2-((S)-1-{2-[3-(3-hydroxymethylbenzyl)ureido]ethyl}pyrrolidin-3-yl)-2,2-diphenylacetamide 

Relevant articles and documents

Compounds having beta2 adrenergic receptor agonist and muscarinic receptor antagonist activity

The invention is directed to compounds of formula I: wherein R1, R2, R3, R4, R5, R6, R7a, R7b, W, G1, G2, a, b, c, d and m are as defined in the specification, or a pharmaceutically acceptable salt or solvate or stereoisomer thereof. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.

Azabicycloalkane compounds

This invention provides compounds of formula I: wherein R1, R2, R3, R4, R5, R6 and R7 are as defined in the specification, or a pharmaceutically acceptable salt or solvate or stereoisomer thereof. The compounds of this invention possess both β2 adrenergic receptor agonist and muscarinic receptor antagonist activity. Such compounds are useful for treating pulmonary disorders, such as chronic obstructive pulmonary disease and asthma.

Substituent effects. 14. Anomalous dissociation constants in water-organic solvent mixtures: benzylammonium ions and related systems

Thermodynamic dissociation constants in various water-organic solvent mixtures are given for benzylammonium, benzyldialkylammonium, and (2-phenylethyl)ammonium ions.Deviations from the Hammett equation (Eqn. 1) are similar to those observed for carboxylic acids, but of opposite sign.The extended Hammett equation (Eqn. 3), containing the hydrophobic constant, ?, yields good correlations.Derived secondary normal sigma values are exemplified.