148625-35-8

Basic information

• Product Name: METHYL 3-FORMYL-4-NITROBENZOATE 97
• Synonyms: METHYL 3-FORMYL-4-NITROBENZOATE 97;AL1HYL 3-FORMYL-4-NITROBENZOATE, 97%;5-Methoxycarbonyl-2-nitrobenzaldehyde;Benzoic acid, 3-forMyl-4-nitro-, Methyl ester;Methyl 3-forMyl-4-nitrobenzoate 97%
• CAS NO: 148625-35-8
• Molecular Formula: C₉H₇NO₅
• Molecular Weight: 209.156
• Product Categories: Aldehydes;C9;Carbonyl Compounds
• Mol File: 148625-35-8.mol
• Article Data: 17

Chemical Properties

• Melting Point: 72-76 °C(lit.)
• Boiling Point: 385.1°C at 760 mmHg
• Flash Point: 193.5°C
• Appearance: /
• Density: 1.386
• Vapor Pressure: 3.91E-06mmHg at 25°C
• Refractive Index: 1.596
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 3-FORMYL-4-NITROBENZOATE 97(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-FORMYL-4-NITROBENZOATE 97(148625-35-8)
• EPA Substance Registry System: METHYL 3-FORMYL-4-NITROBENZOATE 97(148625-35-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 148625-35-8(Hazardous Substances Data)

Usage

General Description

Methyl 3-formyl-4-nitrobenzoate 97 is a chemical compound with the molecular formula C9H7NO5. It is classified under esters, which are organic compounds characterized by an ester group. The '97' in its name means that this chemical is 97% pure; a high level of concentration that attests to its quality. It is a derivative of benzoic acid and has properties in common with other nitrobenzoates. This chemical is primarily used in research and development settings, particularly in the creation of pharmaceuticals and other synthetic processes. Its specific attributes make it suitable for electron transfer studies and reactions.

InChI:InChI=1/C9H7NO5/c1-15-9(12)6-2-3-8(10(13)14)7(4-6)5-11/h2-5H,1H3

Upstream product

• 108763-41-3 methyl (E)-3-(2-(dimethylamino)vinyl)-4-nitrobenzoate 
• 3113-71-1 3-methyl-4-nitrobenzoic acid 
• 143484-14-4 methyl 3-(2-dimethylaminoethenyl)-4-nitrobenzoate 
• 89-87-2 2,4-dimethylnitrobenzene 
• 201932-92-5 methyl 3-(hydroxymethyl)-4-nitrobenzoate 
• 79-37-8 oxalyl dichloride 
• 24078-21-5 methyl 3-methyl-4-nitrobenzoate 
• 207862-97-3 3-dibromomethyl-4-nitrobenzoic acid methyl ester 

Downstream Products

• 886853-92-5 methyl 3-(2,2-dibromovinyl)-4-nitrobenzoate 
• 850074-42-9 2-ethyl 6-methyl benzo[b]thiophene-2,6-dicarboxylate 
• 7345-76-8 dimethyl benzo[b]thiophene-2,5-dicarboxylate 
• 850073-97-1 benzo[b]thiophene-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl ester 
• 841296-15-9 methyl 4-amino-3-formyl-benzoate 
• 1279718-31-8 C₁₀H₁₀N₄O₅ 
• 1536075-06-5 methyl 4-nitro-3-(2,2,2-trichloro-1-hydroxyethyl)benzoate 
• 1426446-50-5 C₁₉H₁₆N₄O₃ 
• 1426446-51-6 C₂₀H₁₈N₄O₃ 
• 1279722-77-8 C₁₉H₁₇N₃O₂ 
• 1279718-18-1 methyl 4-azido-3-formylbenzoate 
• 1283597-18-1 methyl 4-amino-3-(((2-bromobenzyl)(methyl)amino)methyl)benzoate 
• 1283597-32-9 methyl 3-(((2-bromobenzyl)(methyl)amino)methyl)-4-nitrobenzoate 
• 1283597-31-8 methyl 3-((2-bromobenzylamino)methyl)-4-nitrobenzoate 

Relevant articles and documents

Synthesis method for 3-formyl-4-methyl nitrobenzoate

The invention relates to a synthesis method for a compound, in particular to a synthesis method for 3-formyl-4-methyl nitrobenzoate.According to synthesis method, a simple and cheap preparation method for 3-formyl-4-methyl nitrobenzoate is supplied, the reaction conditions in the preparation process are mild, and the yield is high.

Asymmetric total synthesis of martinelline and martinellic acid

Herein, we describe the first asymmetric total synthesis of (-)-martinelline ((-)-2) and the second total synthesis of (-)-martinellic acid ((-)-1) by employing a tandem Mukaiyama-Mannich reaction/aminal cyclization as the key step. The Royal Society of C

FLUORINATED ARYLAMIDE DERIVATIVES

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