Welcome to LookChem.com Sign In|Join Free

CAS

  • or

124506-31-6

Post Buying Request

124506-31-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

124506-31-6 Usage

Description

(R)-Tetrahydrofuran-3-ylmethylamine, also known as (R)-THF-3-ylmethylamine, is a derivative of tetrahydrofuran, a well-known organic compound. It is a member of the tetrahydrofurans, which are heterocyclic compounds with a five-membered ring structure consisting of four carbon atoms and one oxygen atom. The structure and exact properties of this kind of chemical can vary depending on the additional groups attached to the base tetrahydrofuran molecule, although it generally retains a number of important chemical characteristics. Often, these kinds of compounds serve as intermediates in a variety of complex organic syntheses. Stereospecific variants like (R)-Tetrahydrofuran-3-ylmethylamine are an area of considerable research in organic chemistry due to their potential utility in synthesizing other compounds.

Uses

Used in Organic Synthesis:
(R)-Tetrahydrofuran-3-ylmethylamine is used as an intermediate in various complex organic syntheses for its potential utility in synthesizing other compounds. Its unique structure and properties make it a valuable component in the development of new organic molecules.
Used in Pharmaceutical Industry:
(R)-Tetrahydrofuran-3-ylmethylamine is used as a building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents. Its versatility in organic chemistry allows for the creation of diverse molecular structures with potential medicinal applications.
Used in Chemical Research:
(R)-Tetrahydrofuran-3-ylmethylamine is used as a research compound in the field of organic chemistry, where it aids in understanding the properties and reactions of tetrahydrofurans and their derivatives. This knowledge can be applied to the design and synthesis of new compounds with specific characteristics and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124506-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124506-31:
(8*1)+(7*2)+(6*4)+(5*5)+(4*0)+(3*6)+(2*3)+(1*1)=96
96 % 10 = 6
So 124506-31-6 is a valid CAS Registry Number.

124506-31-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Tetrahydrofuran-3-ylmethanol

1.2 Other means of identification

Product number -
Other names [(3R)-oxolan-3-yl]methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:124506-31-6 SDS

124506-31-6Relevant articles and documents

3-(5-METHOXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF

-

Page/Page column 328-329, (2021/06/26)

The present disclosure relates to compounds of formula (I') and pharmaceutical compositions and their use in reducing Widely Interspaced Zinc Finger Motifs (WIZ) expression levels, or inducing fetal hemoglobin (HbF) expression, and in the treatment of inherited blood disorders (e.g., hemoglobinopathies, e.g., beta-hemoglobinopathies), such as sickle cell disease and beta-thalassemia.

Preparation method of tetrahydro-3-furanmethanol

-

Paragraph 0008, (2018/04/02)

The invention relates to the field of preparation of insecticides, in particular to a preparation method of tetrahydro-3-furanmethanol. The method comprises the steps as follows: 13.6 g of sodium ethoxide and 0.5 g of sodium iodide are dissolved in 120 mL of absolute ethyl alcohol, 32 g of diethyl malonate is dropwise added in an ice-water bath, the temperature is controlled at 20 DEG C or below,stirring is performed continuously for 1 h after addition, then 30.3 g of ethyl bromoacetate is slowly added, the temperature is increased to 50-60 DEG C after addition, stirring is performed for about 8 h, ethyl bromoacetate is detected to be used up through gas chromatography, a heating reaction is stopped, the system is cooled to the room temperature, 10 mL of a saturated ammonium chloride solution is added with stirring, the system is adjusted to be neutral or slightly acid, solvent ethyl alcohol is evaporated, residues are dissolved in 100 mL of water and 100 mL of ethyl acetate for extraction, solution separation is performed, an organic phase is separated, the solvent ethyl acetate is removed from the organic phase, reduced pressure distillation is performed through an oil pump, andthe first fraction point, namely, a triethyl 1,1,2-ethanetricarboxylate product, is collected. The process is simple, safety in actual production is guaranteed, and the product with higher yield is obtained.

Production technology for 3-hydroxymethyltetrahydrofuran

-

Paragraph 0033; 0034; 0037; 0043, (2018/10/19)

The invention discloses a production technology for 3-hydroxymethyltetrahydrofuran, and belongs to the field of pesticide intermediate synthetic processes. The production technology is capable of using 2-butene-1,4-diol as a starting raw material, and synthesizing the 3-hydroxymethyltetrahydrofuran through a three-step reaction of dehydration cyclization, hydroformylation and reduction. The production technology is moderate in reaction conditions, low in cost, less in three wastes, and suitable for the industrial production.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 124506-31-6