101093-56-5

Basic information

• Product Name: 2-METHYL 4-BENZYLOXYBENZALDEHYDE
• Synonyms: 4-BENZYLOXY-2-METHYL-BENZALDEHYDE;2-METHYL 4-BENZYLOXYBENZALDEHYDE;Benzaldehyde,2-Methyl-4-(phenylMethoxy)-
• CAS NO: 101093-56-5
• Molecular Formula: C₁₅H₁₄O₂
• Molecular Weight: 226.27
• Mol File: 101093-56-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 58.0 to 62.0 °C
• Boiling Point: 234°C/19mmHg(lit.)
• Flash Point: 176.5 °C
• Appearance: /
• Density: 1.119 g/cm³
• Vapor Pressure: 3.93E-06mmHg at 25°C
• Refractive Index: 1.598
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-METHYL 4-BENZYLOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYL 4-BENZYLOXYBENZALDEHYDE(101093-56-5)
• EPA Substance Registry System: 2-METHYL 4-BENZYLOXYBENZALDEHYDE(101093-56-5)

Safety Data

• Hazardous Substances Data: 101093-56-5(Hazardous Substances Data)

Usage

General Description

2-METHYL 4-BENZYLOXYBENZALDEHYDE is a chemical compound with the molecular formula C16H14O2. It is a benzaldehyde derivative with a benzyl ether and a methyl group attached to the benzene ring. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in organic reactions and as an intermediate in the production of other chemical compounds. It is known to have a sweet, floral aroma and is used in the fragrance industry. 2-METHYL 4-BENZYLOXYBENZALDEHYDE may also have potential applications in the development of new materials and in the field of organic chemistry research.

InChI:InChI=1/C15H14O2/c1-12-9-15(8-7-14(12)10-16)17-11-13-5-3-2-4-6-13/h2-10H,11H2,1H3

Upstream product

• 41438-18-0 4-hydroxy-2-methyl-benzaldehyde 
• 100-44-7 benzyl chloride 
• 17671-75-9 4-(benzyloxy)-1-bromo-2-methylbenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 175153-40-9 methyl 4-benzyloxy-2-methylbenzoate 
• 17819-91-9 4-benzyloxy-2-methylbenzoic acid 
• 100-39-0 benzyl bromide 
• 834-17-3 3-benzyloxytoluene 
• 167479-46-1 4-benzyloxy-2-methylphenylmethanol 
• 52289-54-0 4-methoxysalicylaldehyde 

Downstream Products

• 898538-71-1 4-(benzyloxy)-5-bromo-2-methylbenzaldehyde 
• 17819-91-9 4-benzyloxy-2-methylbenzoic acid 
• 668480-56-6 2-[(4-benzyloxy-2-methyl-phenyl)-hydroxy-methyl]-butyric acid ethyl ester 
• 668477-24-5 (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-methyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one 
• 1048335-58-5 C₂₉H₃₀N₂O₃ 

Relevant articles and documents

Structure-Activity Relationships of cyclo(l -Tyrosyl- l -tyrosine) Derivatives Binding to Mycobacterium tuberculosis CYP121: Iodinated Analogues Promote Shift to High-Spin Adduct

A series of analogues of cyclo(l-tyrosyl-l-tyrosine), the substrate of the Mycobacterium tuberculosis enzyme CYP121, have been synthesized and analyzed by UV-vis and electron paramagnetic resonance spectroscopy and by X-ray crystallography. The introduction of iodine substituents onto cyclo(l-tyrosyl-l-tyrosine) results in sub-μM binding affinity for the CYP121 enzyme and a complete shift to the high-spin state of the heme FeIII. The introduction of halogens that are able to interact with heme groups is thus a feasible approach to the development of next-generation, tight binding inhibitors of the CYP121 enzyme, in the search for novel antitubercular compounds.

DUAL SGLT1/SGLT2 INHIBITORS

The present invention relates to compounds of Formula (I), or a form thereof, wherein A, R1, R2, R3, R4, and R5 are as defined herein, useful as dual SGLT1/SGLT2 inhibitors.

Oxazole derivatives

The present invention relates to novel oxazole compounds which act as PPARα and PPARγ agonists and are accordingly useful for the treatment of diseases modulated by PPARα and PPARγ such as diabetes.