59276-27-6

Basic information

• Product Name: Phenol, 4-(dimethoxymethyl)-
• Synonyms: 4-Hydroxy-benzaldehyd-dimethylacetal;p-hydroxybenzaldehyde dimethyl acetal;4-hydroxy-benzaldehyde dimethylacetal;1,1-dimethoxy-1-(4-hydroxyphenyl)methane;Phenol,4-(dimethoxymethyl)
• CAS NO: 59276-27-6
• Molecular Formula: C9H12O3
• Molecular Weight: 168.192
• Mol File: 59276-27-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Phenol, 4-(dimethoxymethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-(dimethoxymethyl)-(59276-27-6)
• EPA Substance Registry System: Phenol, 4-(dimethoxymethyl)-(59276-27-6)

Safety Data

• Hazardous Substances Data: 59276-27-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 123-08-0 4-hydroxy-benzaldehyde 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 123-08-0 4-hydroxy-benzaldehyde 
• 157284-83-8 2-acetyl-3-(4-hydroxy-phenyl)-acrylic acid methyl ester 
• 42205-38-9 2-cyano-3-(4-hydroxy-phenyl)-acrylic acid ethyl ester 
• 3785-90-8 2-(4-hydroxyphenylmethylene)malononitrile 
• 6935-44-0 ethyl (E)-2-cyano-3-(4-hydroxyphenyl)-2-propenoate 
• 502158-54-5 tris{4-[bis(1,2,4-1H-triazol-1-yl)methyl]phenyl}benzene-1,3,5-tricarboxylate 
• 2538-87-6 trans-p-hydroxycinnamaldehyde 

Relevant articles and documents

Amino acid derivative, feed composition and application thereof

The invention provides an amino acid derivative, a feed composition and application thereof, and belongs to the technical field of animal feed additives. The amino acid derivative is a compound with astructure shown as a formula (I), and a stereoisomer, a tautomer, a solvate, a metabolite, a feed acceptable salt or a prodrug thereof. In formula (I) shown in the specification, Z is a C1-C3 alkylene group. X is an indole ring group with a structure shown as a formula (II). The formula (II) is shown in the specification, wherein Y is phenyl with the structure shown in the formula (III) shown inthe specification. The amino acid derivative is used as an animal feed additive, and can promote the growth of animals and improve the feed conversion.

Phosphorylated Polyacrylonitrile Fibers as an Efficient and Greener Acetalization Catalyst

A novel solid acid catalyst (PANEAPF) is developed by immobilization of phosphoric acid on polyacrylonitrile fiber through covalent bonding. Various characterization techniques such as elemental analysis (EA), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), etc. are utilized to confirm the successful grafting and the stability of the fiber catalysts during application. PANEAPF shows high catalytic activity in the acetalization of aldehydes owing to the high utilization efficiency of its functionalized acid sites. In addition, the strong polarity micro-environment in the surface layers of PANEAPF make it highly suitable for catalytic application in both water and alcohol. Furthermore, the fiber catalyst can be applied to the acetalization of aldehydes in a continuous-flow process at room temperature, and shows excellent reactivity and superior recyclability (over 20 times). The many advantages of PANEAPF such as simple preparation, convenient regulation of acid amount, high durability, and eco-friendly process make it very attractive for fixed-bed reactors in the chemical industry.

An efficient and versatile procedure for the synthesis of acetals from aldehydes and ketones catalyzed by lithium tetrafluoroborate

Acetals are obtained in good to excellent yields by treatment of aldehydes and ketones with trialkyl orthoformate and the corresponding alcohol in the presence of a catalytic amount of lithium tetrafluoroborate. Due to the mild reaction conditions, this method is compatible with acid-sensitive substrates.