184950-35-4

Basic information

• Product Name: (TETRAHYDROFURAN-3-YL)METHANAMINE HYDROCHLORIDE
• Synonyms: (TETRAHYDROFURAN-3-YL)METHANAMINE HYDROCHLORIDE;1-Tetrahydrofuran-3-ylmet...;3-Tetrahydrofuranylmethylamine hydrochloride;Tetrahydro-3-furanmethanamine hydrochloride;(Tetrahydrofuran-3-yl)MethanaMine HCl;(3-Tetrahydrofuranyl)methanamine hydrochloride;3-(Aminomethyl)tetrahydrofuran hydrochloride;oxolan-3-ylmethanamine hydrochloride
• CAS NO: 184950-35-4
• Molecular Formula: C₅H₁₁NO*ClH
• Molecular Weight: 137.61
• EINECS: 1312995-182-4
• Product Categories: Heterocycles series
• Mol File: 184950-35-4.mol

Chemical Properties

• Boiling Point: 200.7 °C at 760 mmHg
• Flash Point: 75.2 °C
• Appearance: /
• Vapor Pressure: 0.268mmHg at 25°C
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: (TETRAHYDROFURAN-3-YL)METHANAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (TETRAHYDROFURAN-3-YL)METHANAMINE HYDROCHLORIDE(184950-35-4)
• EPA Substance Registry System: (TETRAHYDROFURAN-3-YL)METHANAMINE HYDROCHLORIDE(184950-35-4)

Safety Data

• Hazard Codes: Xi
• Statements: 37/38-41
• Safety Statements: 26-39
• Hazardous Substances Data: 184950-35-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(Tetrahydrofuran-3-yl)methanamine hydrochloride is utilized as a building block in the synthesis of a variety of pharmaceuticals and other organic compounds, contributing to the creation of diverse chemical entities for research and development purposes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (Tetrahydrofuran-3-yl)methanamine hydrochloride is employed as a reagent, playing a crucial role in the development of new drugs and the enhancement of existing ones, thereby supporting the advancement of medical treatments.
Used in Polymer Preparation:
(Tetrahydrofuran-3-yl)methanamine hydrochloride also finds application in the preparation of polymers, where it contributes to the formation of polymeric materials with specific properties, useful in various industrial applications.
Used as a Solvent in Chemical Reactions:
Furthermore, (Tetrahydrofuran-3-yl)methanamine hydrochloride is recognized for its use as a solvent in chemical reactions, facilitating the progress of certain processes and potentially improving the yield and efficiency of the reactions it is involved in.

InChI:InChI=1/C5H11NO.ClH/c6-3-5-1-2-7-4-5;/h5H,1-4,6H2;1H

Upstream product

• 79710-86-4 tetrahydrofuran-3-carboxaldehyde 
• 24424-99-5 di-tert-butyl dicarbonate 
• 124391-75-9 3-tetrahydrofuranmethanol 
• 165253-28-1 2-(tetrahydrofuran-3-ylmethyl)-isoindole-1,3-dione 
• 15833-63-3 (tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate 

Relevant articles and documents

AMIDE COMPOUND AND USE THEREOF FOR PEST CONTROL

An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming component(s), one or more atoms or groups that are selected from th

AMIDE COMPOUND AND USE THEREOF FOR PEST CONTROL

An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming component(s), one or more atoms or groups that are selected from th

AMIDE COMPOUND AND USE THEREOF FOR CONTROLLING HARMFUL ARTHROPODS

The present invention provides a novel compound having a control efficacy on harmful arthropods. A compound represented by Formula (I): wherein Y represents a 3-7-membered saturated heterocyclic group containing one or more atoms or groups selected from the group consisting of oxygen atom and -S(O)t- as the heterocycle-constituting element, wherein the saturated heterocyclic group may optionally be substituted with the same or different 1 to 3 atoms or groups selected from Group D; t represents 0 etc.; X represents a phenyl group etc.; W represents an oxygen atom etc.; r represents 0 etc.; R1, R2, R3, R4, R5, R6, R7 and R8 are the same or different to each other and each independently represent hydrogen atom etc.; and n represents 1 etc.; shows an excellent controlling efficacy on harmful arthropods.

DIENE AMIDES AND THEIR USE AGAINST ARTHROPODS

An amide compound represented by the formula (I): [wherein, R1, R2, R3, R4, R5, R6, R7, R8, X, W, r, n and Y are as defined in the description] has an excellent control effect on harmful arthropods.

HETEROARYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

Provided herein are Heteroaryl Compounds having the following structure: (I) wherein R1, R2, L, X, Y, Z, Q, A and B are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.