27065-51-6

Basic information

• Product Name: 4-BroMo-2-diethoxyMethyl-furan
• Synonyms: 4-BroMo-2-diethoxyMethyl-furan
• CAS NO: 27065-51-6
• Molecular Formula: C₉H₁₃BrO₃
• Molecular Weight: 249.10172
• Mol File: 27065-51-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 213.792°C at 760 mmHg
• Flash Point: 83.099°C
• Appearance: /
• Density: 1.352g/cm³
• Vapor Pressure: 0.235mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: 4-BroMo-2-diethoxyMethyl-furan(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BroMo-2-diethoxyMethyl-furan(27065-51-6)
• EPA Substance Registry System: 4-BroMo-2-diethoxyMethyl-furan(27065-51-6)

Safety Data

• Hazardous Substances Data: 27065-51-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H13BrO3/c1-3-11-9(12-4-2)8-5-7(10)6-13-8/h5-6,9H,3-4H2,1-2H3

Upstream product

• 4828-13-1 4,5-dibromo-2-(diethoxymethyl)-furan 
• 21921-76-6 4-bromo-2-furancarbaldehyde 
• 64-17-5 ethanol 
• 2433-85-4 4,5-dibromo-2-furancarboxaldehyde 
• 98-01-1 furfural 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 118608-04-1 methyl (E)-4-hydroxy-2-methoxymethoxy-6-methyl-3<3-methyl-6-<5-(2-methyl-1-propenyl)-3-furanyl>-2-hexenyl>-benzoate 
• 118608-03-0 methyl (E)-2,4-di(methoxymethoxy)-6-methyl-3-<3-methyl-6-<5-(2-methyl-1-propenyl)-3-furanyl>-2-hexenyl>-benzoate 
• 62306-80-3 (5-formylfuran-3-yl)boronic acid 
• 349112-46-5 N-benzyl-N-[4-(methylsulfanyl)-2-furyl]methylamine 
• 639465-53-5 4-methylsulfanyl-2-furaldehyde 
• 118608-02-9 methyl (E)-2,4-di(methoxymethoxy)-6-methyl-3-<3-methyl-6-(furanyl-5-carboxaldehyde)-2-hexenyl>-benzoate 

Relevant articles and documents

IMINO SULFANONE INHIBITORS OF ENPP1

The present disclosure relates generally to inhibitors of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), compositions thereof, and methods of using said compounds and compositions thereof. More specifically, the present disclosure relates to sulfoximine- based inhibitors of ENPP1 of Formula (I) and methods of their use for treating disease mediated by ENPP1.

Synthesis of substituted bis(heteroaryl)maleimides

Substituted bis(fur-2-yl), bis(fur-3-yl) and bis(thien-2-yl) maleimides with potential antidiabetic properties are described. Their synthesis involves, as a key step, a Suzuki cross-coupling between various boron derivatives and the diiodomaleimides. Therefore, a wide range of substituted symmetric and non-symmetric maleimide derivatives can be prepared.

Synthetic routes to cristatic acid and derivatives

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