65658-16-4

Basic information

• Product Name: (2-amino-6-methylphenyl)methanol
• Synonyms: (2-amino-6-methylphenyl)methanol;2-Amino-6-methylbenzyl alcohol
• CAS NO: 65658-16-4
• Molecular Formula: C₈H₁₁NO
• Molecular Weight: 137.17904
• Mol File: 65658-16-4.mol
• Article Data: 17

Chemical Properties

• Melting Point: 85 °C
• Boiling Point: 160-170 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.126±0.06 g/cm3(Predicted)
• PKA: 14.22±0.10(Predicted)
• CAS DataBase Reference: (2-amino-6-methylphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-amino-6-methylphenyl)methanol(65658-16-4)
• EPA Substance Registry System: (2-amino-6-methylphenyl)methanol(65658-16-4)

Safety Data

• Hazardous Substances Data: 65658-16-4(Hazardous Substances Data)

Usage

General Description

(2-amino-6-methylphenyl)methanol is a chemical compound with the molecular formula C8H11NO. It is a white solid with a molecular weight of 137.18 g/mol. (2-amino-6-methylphenyl)methanol is an organic molecule containing an amino group and a hydroxyl group attached to a benzene ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of both an amine and a hydroxyl functional group makes (2-amino-6-methylphenyl)methanol a versatile building block for the production of various compounds. Due to its properties and versatility, it has applications in the pharmaceutical and chemical industries.

Upstream product

• 4389-50-8 2-amino-6-methylbenzoic acid 
• 54915-41-2 2-(hydroxymethyl)-3-methyl-1-nitrobenzene 
• 13506-76-8 2-methyl-6-nitrobenzoic acid 
• 18595-13-6 2-amino-6-methylbenzoic acid methyl ester 
• 61940-22-5 methyl 2-methyl-6-nitrobenzoate 

Downstream Products

• 426216-49-1 1-methyl-11H-dibenzo[b,e]azepine 5-oxide 
• 1472650-01-3 3-methyl-2-(methoxymethyl)-1-aminobenzene 
• 1261794-19-7 (2-iodo-6-methylphenyl)methanol 
• 1261481-48-4 2-(bromomethyl)-1-iodo-3-methylbenzene 
• 1573172-23-2 C₂₂H₂₂IN 
• 1573172-01-6 2-((dibenzylamino)methyl)-3-methylbenzaldehyde 
• 1573171-43-3 (E)-4-(2-((dibenzylamino)methyl)-3-methylphenyl)-1,1,1-trifluorobut-3-en-2-one 

Relevant articles and documents

Facile Access to Triazole-Fused 3,1-Benzoxazines Enabled by Metal-Free Base-Promoted Intramolecular C-O Coupling

A convenient approach to assemble 1,2,3-triazole-fused 4 H -3,1-benzoxazines has been developed. Diverse alcohol-tethered 5-iodotriazoles, readily accessible by a modified protocol of Cu-catalyzed (3+2)-cycloaddition, were utilized as precursors of the target fused heterocycles. The intramolecular C-O coupling proceeded efficiently under base-mediated transition-metal-free conditions, furnishing cyclization products in yields up to 96%. Suppression of the competing reductive cleavage of the C-I bond was achieved by the use of Na 2CO 3in acetonitrile at 100 °C. This practical and cost-effective procedure features a broad substrate scope and valuable functional group tolerance.

Red phosphorescent compound and organic electroluminescent device using same

The invention discloses a red phosphorescent compound and an organic electroluminescent device using the same. In the organic electroluminescent device comprising an anode, a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer and a cathode which are sequentially deposited, a phosphorescent compound as shown in a followingformula I can be used as a dopant of the light emitting layer, wherein R1, R2, R3, R4, R5 and R6 are independently selected from one of H, C1-C6 alkyls and C5-C8 cycloalkyls. The red phosphorescent material is high in efficiency, high in color purity and narrow in spectral effect.

COMPOUNDS AND METHODS FOR REGULATING INSULIN SECRETION

Disclosed herein are methods for inducing insulin secretion in a glucose-dependent manner and compounds for use in these methods.