13527-05-4

Basic information

• Product Name: Benzenemethanol, 4-methyl-, nitrate
• CAS NO: 13527-05-4
• Molecular Formula: C8H9NO3
• Molecular Weight: 167.164
• Mol File: 13527-05-4.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-methyl-, nitrate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-methyl-, nitrate(13527-05-4)
• EPA Substance Registry System: Benzenemethanol, 4-methyl-, nitrate(13527-05-4)

Safety Data

• Hazardous Substances Data: 13527-05-4(Hazardous Substances Data)

Upstream product

• 106-42-3 para-xylene 
• 79439-44-4 C₁₆H₁₈OSe 
• 4484-74-6 4-methylbenzyl iodide 
• 104-84-7 para-methylbenzylamine 
• 76950-85-1 1-(4-Methyl-benzyl)-4,6-diphenyl-1H-pyridine-2-thione 
• 76950-78-2 1-(4-Methyl-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide 
• 73377-43-2 N-(p-Methylbenzyl)-2,4,6-triphenylpyridinium nitrate 
• 104-81-4 4-Methylbenzyl bromide 

Downstream Products

• 589-18-4 4-Methylbenzyl alcohol 
• 104-87-0 4-methyl-benzaldehyde 
• 104-81-4 4-Methylbenzyl bromide 

Relevant articles and documents

Alkyl and aromatic nitrates in atmospheric particles determined by gas chromatography tandem mass spectrometry

Organic nitrates in the atmosphere are associated with photochemical pollution and are the main components of secondary organic aerosols, which are related to haze. An efficient method for determining organic nitrates in atmospheric fine particles (PMsub

Establishment of heterolytic and homolytic Y-NO2 bond dissociation energy scales of nitro-containing compounds in acetonitrile: Chemical origin of NO2 release and capture

(Chemical Equation Presented) The first heterolytic and homolytic N(O)-NO2 bond dissociation energy scales of three types Y-nitro (Y = N, O) compounds and corresponding radical anions in acetonitrile were established by using titration calorimetry combined with relevant electrochemical data through proper thermodynamic cycles.

Mechanistic duality of the side-chain substitution in electrophilic aromatic nitration. Unexpected large difference in deuterium isotope effect k(H)/k(D) between the side-chain nitration and nitrooxylation of deuterated p-xylenes

A large difference in deuterium kinetic isotope effect observed between the side-chain nitration and nitrooxylation of deuterated p-xylenes, 1,4- (CH3)(CD3)C6H4 and 1,4-(CD3)2C6D4, suggests the operation of different mechanisms for these two types of side-chain substitution.