128923-93-3

Basic information

• Product Name: 3'-METHOXY-3-NITROBIPHENYL
• Synonyms: 3'-METHOXY-3-NITROBIPHENYL;3-Methoxy-3'-nitro-1,1'-biphenyl;1-(3-Methoxyphenyl)-3-nitrobenzene
• CAS NO: 128923-93-3
• Molecular Formula: C₁₃H₁₁NO₃
• Molecular Weight: 229.23
• Mol File: 128923-93-3.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3'-METHOXY-3-NITROBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-METHOXY-3-NITROBIPHENYL(128923-93-3)
• EPA Substance Registry System: 3'-METHOXY-3-NITROBIPHENYL(128923-93-3)

Safety Data

• Hazardous Substances Data: 128923-93-3(Hazardous Substances Data)

Usage

General Description

3'-Methoxy-3-nitrobiphenyl is a chemical compound with the molecular formula C13H11NO3. It is a yellow crystalline solid with a melting point of around 64-65°C. This chemical is used primarily as an intermediate in the synthesis of dyes and pigments, as well as in the production of pharmaceuticals and organic compounds. It is classified as a nitrobiphenyl, which is a type of organic compound containing a biphenyl ring system with one or more nitro groups attached. 3'-Methoxy-3-nitrobiphenyl is known to be harmful if swallowed or inhaled, and precautions should be taken when handling this substance.

Upstream product

• 554-84-7 meta-nitrophenol 
• 10365-98-7 3-methoxyphenylboronic acid 
• 80858-83-9 3-nitrophenoxysulfonyl fluoride 
• 2845-89-8 1-chloro-3-methoxy-benzene 
• 13331-27-6 m-nitrobenzene boronic acid 
• 2398-37-0 3-methoxyphenyl bromide 
• 66107-33-3 3-methoxyphenyl triflate 
• 18312-48-6 potassium m-nitrobenzoate 
• 645-00-1 m-iodonitrobenzene 
• 958-96-3 3,3'-dinitro-1,1'-biphenyl 
• 124-41-4 sodium methylate 
• 585-79-5 m-nitrobromobenzene 

Downstream Products

• 136539-67-8 1‐(3‐hydroxyphenyl)‐3‐nitrobenzene 
• 400748-70-1 3‘-methoxy-[1,1‘-biphenyl]-3-amine 

Relevant articles and documents

A green synthesis of biaryls in water catalyzed by palladium nanoparticles immobilized on N-amidinoglycine-functionalized iron oxide nanoparticles

Fe3O4 nanoparticles were prepared by co-precipitation and coated with SiO2 following the St?ber process. N-Amidinoglycine amino acid was then covalently connected to provide an excellent ligand for the immobilization of Pd nanoparticles. The resulting material was characterized by FE-SEM, TEM, EDX, XRD, VSM and ICP-AES analysis. The Fe3O4@SiO2@N-amidinoglycine@Pd0 proved to be a highly active catalyst for the Suzuki coupling reactions of various aryl halides with substituted phenylboronic acids in water, giving the desired products in excellent yields for short reaction times. Moreover, this catalyst can be easily recovered by using an external magnet and directly reused for several times without significant loss of activity.

SUBSTITUTED BICYCLIC COMPOUNDS AS FARNESOID X RECEPTOR MODULATORS

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Triazole carbene palladium metal coordination compound, preparation method and applications thereof

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