136507-14-7

Basic information

• Product Name: 2-METHOXY-4-NITROBENZYL ALCOHOL
• Synonyms: 2-METHOXY-4-NITROBENZYL ALCOHOL
• CAS NO: 136507-14-7
• Molecular Formula: C₈H₉NO₄
• Molecular Weight: 183.16
• Mol File: 136507-14-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 357.4 °C at 760 mmHg
• Flash Point: 169.95 °C
• Appearance: /
• Density: 1.317 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.574
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-METHOXY-4-NITROBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXY-4-NITROBENZYL ALCOHOL(136507-14-7)
• EPA Substance Registry System: 2-METHOXY-4-NITROBENZYL ALCOHOL(136507-14-7)

Safety Data

• Hazardous Substances Data: 136507-14-7(Hazardous Substances Data)

Usage

General Description

2-Methoxy-4-nitrobenzyl alcohol is a chemical compound with the molecular formula C8H9NO4. It is commonly used as a reagent in organic synthesis and as a precursor in the production of various pharmaceuticals and agrochemicals. 2-Methoxy-4-nitrobenzyl alcohol is characterized by its pale yellow crystalline appearance and is soluble in organic solvents such as ethanol and methanol. It is also known for its strong odor and should be handled with caution due to its potential to cause irritation to the skin, eyes, and respiratory system. 2-Methoxy-4-nitrobenzyl alcohol is most commonly used in the synthesis of various pharmaceutical compounds and has applications in the pharmaceutical and agricultural industries.

InChI:InChI=1/C8H9NO4/c1-13-8-4-7(9(11)12)3-2-6(8)5-10/h2-4,10H,5H2,1H3

Upstream product

• 136507-13-6 acetic acid 2-methoxy-4-nitro-benzyl ester 
• 136507-15-8 4-nitro-2-methoxybenzaldehyde 
• 1009-36-5 2-chloro-5-nitroanisole 
• 619-19-2 2-hydroxy-4-nitrobenzoic acid 
• 2597-56-0 4-nitro-o-anisic acid 
• 90434-16-5 1-(bromomethyl)-2-methoxy-4-nitrobenzene 
• 13120-77-9 2-methyl-5-nitroanisole 
• 39106-79-1 methyl 2-methoxy-4-nitrobenzoate 

Downstream Products

• 622863-80-3 5-(benzyloxy)-2-[(E)-2-(2-methoxy-4-nitrophenyl)ethenyl]-1H-indole 
• 622858-54-2 9-hydroxy-4-(2-methoxy-4-nitrophenyl)pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione 
• 622863-82-5 9-benzyloxy-4-(2-methoxy-4-nitro-phenyl)-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione 
• 622863-84-7 9-benzyloxy-4-(2-methoxy-4-nitrophenyl)pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione 
• 1254102-40-3 4-(((tert-butyldimethylsilyl)oxy)methyl)-3-methoxyaniline 
• 1425051-86-0 C₂₁H₂₉NO₄Si 
• 1425052-02-3 C₂₉H₄₄BNO₇Si 
• 1425051-88-2 C₂₃H₃₀BNO₇ 
• 1425051-90-6 C₃₀H₃₄BN₃O₁₀ 
• 1425052-03-4 C₃₈H₅₃BN₂O₁₀Si 
• 1425052-04-5 C₃₂H₃₉BN₂O₁₀ 
• 1425051-91-7 C₃₉H₄₃BN₄O₁₃ 
• 1425051-84-8 tert-butyl((2-methoxy-4-nitrobenzyl)oxy)dimethylsilane 
• 882430-21-9 tert-butyl(3-methoxy-4-nitrobenzyloxy)dimethylsilane 

Relevant articles and documents

Development of Bioreduction Labile Protecting Groups for the 2′-Hydroxyl Group of RNA

Protection and deprotection of the 2′-hydroxyl group of RNAs are critical for RNA-based drug discovery. This paper reports development of a bioreduction labile protecting group of the 2′-hydroxyl group in RNA. After the reduction of the nitro group in a c

PYRROLONE OR PYRROLIDINONE MELANIN CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS

The present invention provides compounds of Formula (I): as defined in the specification and compositions comprising any of such novel compounds. These compounds are melanin concentrating hormone receptor-1 (MCHR1) antagonists which may be used as medicaments.

Palladium-catalyzed direct hydroxymethylation of aryl halides and triflates with potassium acetoxymethyltrifluoroborate

Suzuki-Miyaura cross-coupling reactions of aryl halides and triflates with potassium acetoxymethyltrifluoroborate afforded the corresponding aryl and heteroaryl methanol products in moderate to excellent yields.