50347-17-6

Basic information

• Product Name: 6-METHYLAMINOHEXAN-1-OL
• Synonyms: 6-METHYLAMINOHEXAN-1-OL;6-METHYLAMINOHEXANOL-1;TIMTEC-BB SBB008548;6-Methylaminohexanol;6-METHYLAMINOHEXAN-1-OL 95%
• CAS NO: 50347-17-6
• Molecular Formula: C₇H₁₇NO
• Molecular Weight: 131.22
• Mol File: 50347-17-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 200.282°C at 760 mmHg
• Flash Point: 62.403°C
• Appearance: /
• Density: 0.872g/cm³
• Vapor Pressure: 0.081mmHg at 25°C
• Refractive Index: 1.44
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 15.19±0.10(Predicted)
• CAS DataBase Reference: 6-METHYLAMINOHEXAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 6-METHYLAMINOHEXAN-1-OL(50347-17-6)
• EPA Substance Registry System: 6-METHYLAMINOHEXAN-1-OL(50347-17-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 50347-17-6(Hazardous Substances Data)

Usage

General Description

6-Methylaminohexan-1-ol is a chemical compound with the molecular formula C7H17NO. It is a primary amine and an alcohol, which means it contains both an amino group and a hydroxyl group. 6-METHYLAMINOHEXAN-1-OL is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. It may also be used as a precursor in the manufacturing of other chemicals. In addition, 6-Methylaminohexan-1-ol has potential applications in the fragrance and flavor industries, where it can be used to create unique scent profiles. Overall, this compound has diverse uses and is an important intermediate in the production of a wide range of chemical products.

InChI:InChI=1/C7H17NO/c1-8-6-4-2-3-5-7-9/h8-9H,2-7H2,1H3

Upstream product

• 67-56-1 methanol 
• 4048-33-3 6-amino-1-hexanol 
• 2556-73-2 1-methyl-2-azepanone 
• 75937-12-1 6-(Boc-amino)-1-hexanol 
• 60-32-2 6-aminohexanoic acid 
• 4143-15-1 6-(N-ethoxycarbonylamino)hexanoic acid 
• 2009-83-8 6-chloro-1-hexanol 
• 74-89-5 methylamine 

Downstream Products

• 1862-07-3 6-(N,N-dimethylamino)-1-hexanol 
• 55863-02-0 N-methylhex-5-en-1-amine 

Relevant articles and documents

HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

Ligand, metal complex containing ligand, and reaction using metal complex containing ligand

A hydrogen transfer reaction may be more efficiently promoted by using a metal complex represented by Formula (2): (wherein, R1 to R8 are the same or different, and each represents a hydrogen atom, a substituted or unsubstituted alkyl group or the like; or wherein; R1 and R2, R2 and R3, R3 and R4, R4 and R5, and R5 and R6 are respectively bonded to each other to form a bivalent hydrocarbon group; R9 are the same or different, and each represents an alkyl group or cycloalkyl group; M is ruthenium (Ru) or the like; X is a ligand; and n is 0, 1 or 2). More specifically, the metal complex enables a hydrogenation reaction of various substrates having a stable carbonyl group or the like to be advanced with a high yield under mild conditions.

BI-FUNCTIONAL QUINOLINE ANALOGS

Provided are compounds of Formula I: wherein X is: R1 and R2 together with the phenyl to which they are bound may form a bicyclic, fused heterocyclic ring, and all other variables are as defined herein, as well as their use in treating pulmonary inflammation or bronchoconstriction and compositions comprising and processes for preparing the same.