17743-37-2

Basic information

• Product Name: 3-hydroxy-2,4,6-trimethylbenzaldehyde
• Synonyms: 3-hydroxy-2,4,6-trimethylbenzaldehyde
• CAS NO: 17743-37-2
• Molecular Weight: 164.204
• Mol File: 17743-37-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-2,4,6-trimethylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-2,4,6-trimethylbenzaldehyde(17743-37-2)
• EPA Substance Registry System: 3-hydroxy-2,4,6-trimethylbenzaldehyde(17743-37-2)

Safety Data

• Hazardous Substances Data: 17743-37-2(Hazardous Substances Data)

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 
• 224641-82-1 3-hydroxy-2,4,6-triiodobenzaldehyde 
• 594-27-4 tetramethylstannane 
• 70682-52-9 (RS)-6-Acetoxy-2,3,4,6-tetramethyl-2,4-cyclohexadien-1-on 
• 74-90-8 hydrogen cyanide 
• 4028-66-4 2,4,6-trimethylanisole 
• 527-60-6 Mesitol 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 17743-36-1 3-hydroxy-2,4,6-trimethyl-benzyl alcohol 
• 1354003-04-5 2,4,6-trimethyl-3-(2-(2-oxoimidazolidin-1-yl)ethoxy)nitrile oxide 
• 1354003-01-2 2,4,6-trimethyl-3-(2-(2-oxoimidazolidin-1-yl)ethoxy)benzaldehyde oxime 
• 1354003-00-1 2,4,6-trimethyl-3-(2-(2-oxoimidazolidin-1-yl)ethoxy)benzaldehyde 
• 135778-94-8 3-Hydroxy-2,4,6-trimethyl-benzonitrile N-oxide 
• 135778-88-0 3-Hydroxy-2,4,6-trimethyl-benzaldehyde oxime 

Relevant articles and documents

COMPOUND, PHOTOPOLYMERIZATION INITIATOR, PHOTOCURABLE COMPOSITION AND CURED PRODUCT THEREOF, AND PHOTOCURABLE INK AND PRINT USING THE SAME

There are provided a compound represented by general formula (1), a photopolymerization initiator comprising this compound, a photocurable composition having this photopolymerization initiator and a photocurable compound as essential components, and a cur

Graft polymer to which combined nitrogen molecules are grafted

The present invention relates to a modified polymer obtained by grafting of a compound comprising at least one group Q and at least one group A, bonded together by at least, and preferably, one “spacer” group Sp in which: Q comprises a dipole containing at least, and preferably, one nitrogen atom, capable of being grafted onto the polymer chain by [1,3]-dipolar cycloaddition,A comprises an associative group comprising at least one nitrogen atom,Sp is an atom or a group of atoms forming a bond between Q and A.

SYNTHESIS OF STERICALLY HINDERED AROMATIC ALDEHYDES

Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4.A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.