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2-(Tetrahydrofuran-2-yl)ethanamine, a chemical compound with the molecular formula C6H13NO, is an amine that features a tetrahydrofuran ring and an ethylamine group. It is recognized for its unique structure and reactivity, which makes it a promising building block in the construction of complex organic molecules. 2-(TETRAHYDROFURAN-2-YL)ETHANAMINE is also notable for its potential applications in medicinal chemistry and chemical biology.

98277-97-5

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98277-97-5 Usage

Uses

Used in Organic Synthesis:
2-(Tetrahydrofuran-2-yl)ethanamine is used as a versatile intermediate in organic synthesis for its ability to contribute to the formation of a wide range of complex organic molecules. Its unique structure allows it to participate in various chemical reactions, facilitating the synthesis of desired compounds.
Used in Drug Development:
In the pharmaceutical industry, 2-(Tetrahydrofuran-2-yl)ethanamine is utilized as a key component in drug development. Its incorporation into drug molecules can enhance their pharmacological properties, such as potency, selectivity, and bioavailability, making it an important player in the creation of new therapeutic agents.
Used in Pharmaceutical Production:
2-(Tetrahydrofuran-2-yl)ethanamine is used as a building block in the production of pharmaceuticals. Its unique structural features and reactivity contribute to the development of novel drug molecules with improved therapeutic profiles.
Used in Agrochemicals:
In the agrochemical industry, 2-(Tetrahydrofuran-2-yl)ethanamine is used in the development of new agrochemicals. Its potential to be incorporated into molecules with specific pesticidal or herbicidal properties makes it a valuable compound in this field.
Used in Medicinal Chemistry:
2-(Tetrahydrofuran-2-yl)ethanamine is used as a component in medicinal chemistry for its potential to be part of molecules with biological activity. Its unique structure can be leveraged to design drugs that target specific biological pathways or receptors.
Used in Chemical Biology:
In chemical biology, 2-(Tetrahydrofuran-2-yl)ethanamine may have applications in the study of biological processes and the development of bioactive molecules. Its unique properties can be harnessed to probe and modulate biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 98277-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,7 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98277-97:
(7*9)+(6*8)+(5*2)+(4*7)+(3*7)+(2*9)+(1*7)=195
195 % 10 = 5
So 98277-97-5 is a valid CAS Registry Number.

98277-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(oxolan-2-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 2-oxolan-2-ylethylamine

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:98277-97-5 SDS

98277-97-5Relevant academic research and scientific papers

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 1378; 1379; 1380, (2019/02/13)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Pyrimidine derivatives as IL-8 receptor antagonists

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Page 27, (2010/02/06)

Compounds containing the pyrimidine nucleus and their use to treat diseases and conditions related to inappropriate Interleukin-8 receptor activity are disclosed. The compounds are of the formula I In these compounds, Q is preferably unsubstituted and substituted heterocyclyl; U is usually hydrogen or fluorine; and V is preferably hydrogen, halogen, alkyl, —O—alkyl or —S-alkyl. A representative example is:

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