480439-09-6

Basic information

• Product Name: 5-(4-CHLORO-2-NITROPHENYL)FURFURAL 97
• Synonyms: 5-(4-CHLORO-2-NITROPHENYL)FURFURAL 97
• CAS NO: 480439-09-6
• Molecular Formula: C₁₁H₆ClNO₄
• Molecular Weight: 251.624
• Product Categories: API intermediates;Building Blocks;Furans;FuransHeterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks
• Mol File: 480439-09-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 91-95 °C(lit.)
• Boiling Point: 402.2°Cat760mmHg
• Flash Point: 197°C
• Appearance: /
• Density: 1.454g/cm³
• Vapor Pressure: 1.12E-06mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: 5-(4-CHLORO-2-NITROPHENYL)FURFURAL 97(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-CHLORO-2-NITROPHENYL)FURFURAL 97(480439-09-6)
• EPA Substance Registry System: 5-(4-CHLORO-2-NITROPHENYL)FURFURAL 97(480439-09-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 480439-09-6(Hazardous Substances Data)

Usage

Properties

1. Chemical formula: C10H5ClNO4
2. Molecular weight: 229.61 g/mol
3. Purity: 97%
4. Intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes
5. Potential applications in organic chemistry as a reagent or building block

Specific content

1. Chlorine and nitro group substituted on the phenyl ring
2. Used as an intermediate in various industries
3. Suitable for research and industrial applications due to 97% purity
4. Molecular formula: C10H5ClNO4

InChI:InChI=1/C11H6ClNO4/c12-7-1-3-9(10(5-7)13(15)16)11-4-2-8(6-14)17-11/h1-6H

Upstream product

• 98-01-1 furfural 
• 89-63-4 4-Chloro-2-nitroaniline 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 6280-88-2 4-chloro-2-nitro-benzoic acid 

Downstream Products

• 1287721-80-5 C₂₃H₁₅ClN₄O₄S₂ 
• 1282538-96-8 2-[1-(4-isobutylphenyl)ethyl]-5-[(5-(4-chloro-2-nitrophenyl)furan-2-yl)methylidene]-[1,3]thiazolo[3,2-b]-1,2,4-triazol-6(5H)-one 
• 1391113-78-2 C₂₁H₁₆ClNO₆ 
• 1391114-08-1 2-[1-{5-(5-(4-chloro-2-nitrophenyl)furan-2-yl)-3-(2,4-dimethoxyphenyl)-4,5-dihydro-1H-pyrazolyl}]-4-(4-nitrophenyl)[1,3]thiazole 
• 1391113-92-0 C₂₂H₁₉ClN₄O₅S 
• 95611-88-4 5-(4-chloro-2-nitrophenyl)-2-furoic acid 

Relevant articles and documents

Derivatives of (R)-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific Activity

NMDA receptors mediate glutamatergic neurotransmission and are therapeutic targets due to their involvement in a variety of psychiatric and neurological disorders. Here, we describe the design and synthesis of a series of (R)-3-(5-furanyl)carboxamido-2-am

Palladium-catalyzed decarboxylative C-H bond arylation of furans

A Pd/PCy3/Ag2CO3 (Cy = cyclohexyl) catalytic system was found to promote decarboxylative arylation through the combination of decarboxylation and C-H bond functionalization. This protocol features a good substrate scope of

Furan as a 1,3-diketone equivalent: the second type furan recyclization applied to indole synthesis

A new approach for the synthesis of indole derivatives based on protolytic recyclization of 2-alkyl-5-(2-tosylaminoaryl)-furans is described. The furan ring in this unusual transformation formally serves as a 1,3-diketone equivalent.