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3-(2-furyl)propan-1-amine oxalate is a chemical compound that features a furyl ring attached to a propan-1-amine backbone, with an oxalate group forming a salt with the amine. 3-(2-furyl)propan-1-amine oxalate is known for its aromatic properties due to the furyl ring and its reactivity due to the amine functional group. The oxalate salt form enhances the stability and solubility of the compound in various solvents, facilitating its use in laboratory settings.

4428-38-0

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4428-38-0 Usage

Uses

Used in Chemical Synthesis:
3-(2-furyl)propan-1-amine oxalate is used as a reagent in chemical synthesis for the preparation of various organic compounds. Its unique structure allows for versatile reactions with other compounds, making it a valuable component in the synthesis of a wide range of products.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 3-(2-furyl)propan-1-amine oxalate is used as a building block for the development of new drugs. Its aromatic and amine properties can be leveraged to create molecules with potential therapeutic effects.
Used in Agrochemical Research and Development:
3-(2-furyl)propan-1-amine oxalate also finds application in the agrochemical sector, where it is utilized in the research and development of new pesticides, herbicides, and other agricultural chemicals. Its chemical properties make it a promising candidate for the creation of effective and targeted agrochemicals.
Used in Material Science Research and Development:
In the field of material science, 3-(2-furyl)propan-1-amine oxalate is employed for the development of new materials with specific properties. Its ability to participate in various chemical reactions allows for the creation of materials with tailored characteristics for use in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4428-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4428-38:
(6*4)+(5*4)+(4*2)+(3*8)+(2*3)+(1*8)=90
90 % 10 = 0
So 4428-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c8-5-1-3-7-4-2-6-9-7/h2,4,6H,1,3,5,8H2

4428-38-0 Well-known Company Product Price

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  • Aldrich

  • (CBR00236)  3-(2-Furyl)-1-propanamine  AldrichCPR

  • 4428-38-0

  • CBR00236-1G

  • 3,540.42CNY

  • Detail

4428-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Furyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names 3-furan-2-yl-propylamine

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:4428-38-0 SDS

4428-38-0Relevant academic research and scientific papers

Synthesis of spirocyclic azacycles from the cyclization of furan tethered N-acyliminium ions

Shengule, Sudhir R.,Willis, Anthony,Pyne, Stephen G.

, p. 1207 - 1215 (2012/02/16)

The protic and Lewis acid promoted cyclization reactions of tethered furan-4,5-dihydroxypiperid-2-ones, furan-4,5-diacetoxypiperid-2-ones and furan-3,4-diacetoxypyrrolid-2-ones, via their corresponding N-acyliminium ion intermediates, have been studied. I

Pyrimidine derivatives as IL-8 receptor antagonists

-

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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