192819-68-4

Basic information

• Product Name: Benzaldehyde, 3-(chloromethyl)-2-hydroxy-5-methyl- (9CI)
• Synonyms: Benzaldehyde, 3-(chloromethyl)-2-hydroxy-5-methyl- (9CI);3-(Chloromethyl)-2-hydroxy-5-methylbenzaldehyde
• CAS NO: 192819-68-4
• Molecular Formula: C₉H₉ClO₂
• Molecular Weight: 184.61956
• Product Categories: HALOMETYL
• Mol File: 192819-68-4.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzaldehyde, 3-(chloromethyl)-2-hydroxy-5-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3-(chloromethyl)-2-hydroxy-5-methyl- (9CI)(192819-68-4)
• EPA Substance Registry System: Benzaldehyde, 3-(chloromethyl)-2-hydroxy-5-methyl- (9CI)(192819-68-4)

Safety Data

• Hazardous Substances Data: 192819-68-4(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 106-44-5 p-cresol 
• 140875-58-7 (2,2,6-trimethyl-4H-benzo[1,3]dioxin-8-yl)-methanol 
• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 
• 140875-59-8 6-formyl-4-methylsalicyl alcohol isopropylidene acetal 

Downstream Products

• 65448-72-8 2-hydroxy-3-(hydroxymethyl)-5-methylbenzaldehyde 
• 301152-69-2 C₂₇H₃₇N₃O₂ 
• 1428521-93-0 3-((bis(2-hydroxyethyl)-amino)methyl)-2-hydroxy-5-methylbenzaldehyde 

Relevant articles and documents

Synthesis of asymmetric N-arylaziridine derivatives using a new chiral phase-transfer catalyst

Substituted N-arylaziridine derivatives were synthesized in an enantioselective manner from N-acyl-N-arylhydroxylamine and electron deficient olefins using chiral phase-transfer catalysts (CPTCs) derived from cinchona alkaloids. The structures of the CPTC

In Situ Ligand Formation in the Synthetic Processes from Mononuclear Dy(III) Compounds to Binuclear Dy(III) Compounds: Synthesis, Structure, Magnetic Behavior, and Theoretical Analysis

Guided by the self-assembled process and mechanism, the strategy of in situ Schiff base reaction would be capable of bringing a feasible method to construct and synthesize lanthanide compounds with distinct structures and magnetic properties. A mononuclea

Design, synthesis and evaluation of new classes of nonquaternary reactivators for acetylcholinesterase inhibited by organophosphates

A new series of nonquaternary conjugates for reactivation of both nerve agents and pesticides inhibited hAChE were described in this paper. It was found that substituted salicylaldehydes conjugated to aminobenzamide through piperidine would produce efficient reactivators for sarin, VX and tabun inhibited hAChE, such as L6M1R3, L6M1R5 to L6M1R7, L4M1R3 and L4M1R5 to L4M1R7. The in vitro reactivation experiment for pesticides inhibited hAChE of these new synthesized oximes were conducted for the first time. Despite they were less efficient than obidoxime, some of them were highlighted as equal or more efficient reactivators in comparison to 2-PAM. It was found that introduction of peripheral site ligands could increase oximes’ binding affinity for inhibited hAChE in most cases, which resulted in greater reactivation ability.