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2-Furanmethanamine, alpha-ethyl-4-(1-methylethyl)-, (alphaR)-(9CI), also known as (R)-2-ethyl-4-isopropyl-1-aminobutan-1-ol, is a chemical compound with the molecular formula C9H15NO. It is an amine derivative of furan, featuring a butylamine substituent. 2-Furanmethanamine,alpha-ethyl-4-(1-methylethyl)-,(alphaR)-(9CI) is primarily utilized in laboratory research and may hold potential for pharmaceutical development and organic synthesis. Further study and testing are required to determine its specific properties and potential applications.

473733-02-7

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473733-02-7 Usage

Uses

Used in Pharmaceutical Development:
2-Furanmethanamine, alpha-ethyl-4-(1-methylethyl)-, (alphaR)-(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a promising candidate for the development of new drugs with novel therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Furanmethanamine, alpha-ethyl-4-(1-methylethyl)-, (alphaR)-(9CI) serves as a versatile building block for the creation of complex organic molecules. Its amine functionality allows for a wide range of chemical reactions, enabling the synthesis of diverse organic compounds with potential applications in various industries.
Used in Laboratory Research:
2-Furanmethanamine, alpha-ethyl-4-(1-methylethyl)-, (alphaR)-(9CI) is employed as a research tool in laboratories to study its chemical properties, reactivity, and potential applications. Researchers use 2-Furanmethanamine,alpha-ethyl-4-(1-methylethyl)-,(alphaR)-(9CI) to explore new reaction pathways, develop innovative synthetic methods, and gain insights into the structure-activity relationships of related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 473733-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,7,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 473733-02:
(8*4)+(7*7)+(6*3)+(5*7)+(4*3)+(3*3)+(2*0)+(1*2)=157
157 % 10 = 7
So 473733-02-7 is a valid CAS Registry Number.

473733-02-7SDS

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 (1R)-1-(4-propan-2-ylfuran-2-yl)propan-1-amine

1.2 Other means of identification

Product number -
Other names (R)-1-(4-isopropylfuran-2-yl)propan-1-amine

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:473733-02-7 SDS

473733-02-7Downstream Products

473733-02-7Relevant articles and documents

C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists

Chao, Jianhua,Taveras, Arthur G.,Chao, Jianping,Aki, Cynthia,Dwyer, Michael,Yu, Younong,Purakkattle, Biju,Rindgen, Diane,Jakway, James,Hipkin, William,Fosetta, James,Fan, Xuedong,Lundell, Daniel,Fine, Jay,Minnicozzi, Michael,Phillips, Jonathan,Merritt, J. Robert

, p. 3778 - 3783 (2008/02/10)

A novel series of cyclobutenedione centered C(4)-alkyl substituted furanyl analogs was developed as potent CXCR2 and CXCR1 antagonists. Compound 16 exhibits potent inhibitory activities against IL-8 binding to the receptors (CXCR2 Ki = 1 nM, IC50 = 1.3 nM; CXCR1 Ki = 3 nM, IC50 = 7.3 nM), and demonstrates potent inhibition against both Gro-α and IL-8 induced hPMN migration (chemotaxis: CXCR2 IC50 = 0.5 nM, CXCR1 IC50 = 37 nM). In addition, 16 has shown good oral pharmacokinetic profiles in rat, mouse, monkey, and dog.

THIADIAZOLEDIOXIDES AND THIADIAZOLEOXIDES AS CXC- AND CC-CHEMOKINE RECEPTOR LIGANDS

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Page 263, (2008/06/13)

Disclosed are novel compounds of the formula (IA) and the pharmaceutically acceptable salts and solvates thereof. Examples of groups comprising Substituent A include heteroaryl, aryl, heterocycloalkyl, cycloalkyl, aryl, alkynyl, alkenyl, aminoalkyl, alkyl or amino. Examples of groups comprising Substituent B include aryl and heteroaryl. Also disclosed is a method of treating a chemokine mediated diseases, such as, cancer, angiogenisis, angiogenic ocular diseases, pulmonary diseases, multiple sclerosis, rheumatoid arthritis, osteoarthritis, stroke and cardiac reperfusion injury, acute pain, acute and chronic inflammatory pain, and neuropathic pain using a compound of formula (IA).

3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands

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Page 136; 139, (2008/06/13)

There are disclosed compounds of the formula or a pharmaceutically acceptable salt or solvate thereof which are useful for the treatment of chemokine-mediated diseases such as acute and chronic inflammatory disorders and cancer.

3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands

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Page 139, (2008/06/13)

There are disclosed compounds of the formula or a pharmaceutically acceptable salt or solvate thereof which are useful for the treatment of chemokine-mediated diseases such as acute and chronic inflammatory disorders and cancer.

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