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124506-31-6

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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

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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.

Robust cobalt oxide catalysts for controllable hydrogenation of carboxylic acids to alcohols

Song, Song,Wang, Dong,Di, Lu,Wang, Chuanming,Dai, Weili,Wu, Guangjun,Guan, Naijia,Li, Landong

, p. 250 - 257 (2018/02/20)

The selective catalytic hydrogenation of carboxylic acids is an important process for alcohol production, while efficient heterogeneous catalyst systems are still being explored. Here, we report the selective hydrogenation of carboxylic acids using earth-abundant cobalt oxides through a reaction-controlled catalysis process. The further reaction of the alcohols is completely hindered by the presence of carboxylic acids in the reaction system. The partial reduction of cobalt oxides by hydrogen at designated temperatures can dramatically enhance the catalytic activity of pristine samples. A wide range of carboxylic acids with a variety of functional groups can be converted to the corresponding alcohols at a yield level applicable to large-scale production. Cobalt monoxide was established as the preferred active phase for the selective hydrogenation of carboxylic acids.

Insecticide dinotefuran intermediate 3 - hydroxy methyl tetrahydrofuran synthetic method

-

, (2018/04/01)

The invention discloses a synthetic method of pesticide dinotefuran intermediate 3-hydroxymethyl tetrahydrofuran, and the synthetic method is as follows: reacting compound succinic acid dialkyl ester with formic acid alkyl ester in the presence of a strong alkali to obtain a compound III, then obtaining a compound II by a reduction reaction, finally, in the presence of an acid catalyst, obtaining a compound shown as formula I by a dehydration cyclization reaction, and R or R ' respectively independently represents C1-5 alkyl. The synthetic method is low in raw material cost, simple in reaction operation, less in pollution, high in yield of each step, 99% in the yield of the reducing step, and suitable for industrial production.

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