80459-46-7

Basic information

• Product Name: Benzaldehyde, 3-[[(4-methylphenyl)sulfonyl]oxy]-
• CAS NO: 80459-46-7
• Molecular Formula: C14H12O4S
• Molecular Weight: 276.313
• Mol File: 80459-46-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 3-[[(4-methylphenyl)sulfonyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3-[[(4-methylphenyl)sulfonyl]oxy]-(80459-46-7)
• EPA Substance Registry System: Benzaldehyde, 3-[[(4-methylphenyl)sulfonyl]oxy]-(80459-46-7)

Safety Data

• Hazardous Substances Data: 80459-46-7(Hazardous Substances Data)

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 
• 98-59-9 p-toluenesulfonyl chloride 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1425968-54-2 2,5,9-trioxa-1⁴-benzoyl-1,4(1,3),7(1,4)-tribenzena cyclononaphane 
• 1425968-57-5 3,7,10-trioxa-1³-phenyl-1(2,6)-benzofurana-2,8(1,3),5(1,4)-tribenzenacyclodecaphane 
• 1425968-58-6 2-oxo-5,8-dioxa-1⁶-benzoyl-1,6(1,3),3(1,4)-tribenzena cyclooctaphane 
• 1425968-59-7 5,8-dioxa-1⁶-benzoyl-2-hydroxy-1,6(1,3),3(1,4)-tribenzenacyclooctaphane 
• 1425968-55-3 3-(tosyloxy)benzyl alcohol 
• 1425968-56-4 2,4-bis[3'-(hydroxyl)benzyloxy]benzophenone 
• 1425968-62-2 2-hydroxy-4-[3′-(tosyloxy)benzyloxy]benzophenone 
• 1425968-63-3 2-hydroxy-4-[3'-(hydroxy)benzyloxy]benzophenone 
• 1425968-53-1 3,5,8,12-tetraoxa-4⁴-benzoyl-1,4,7(1,3),10(1,4)-tetrabenzenacyclododecaphane 
• 7070-85-1 3-[1,3]dioxolan-2-yl-phenol 
• 135879-40-2 3,3'-oxybis(benzaldehyde) 

Relevant articles and documents

Thiazole amide compound and preparation method, pharmaceutical composition and application thereof

The invention discloses a thiazole amide compound and a preparation method thereof, a pharmaceutical composition and application thereof. The thiazole amide compound as shown in a formula I and a pharmaceutically acceptable salt thereof are provided, and

Cyclophane size drives the photochemical behaviour of benzophenone

A new series of all-heterahomocalixarene-type structures was prepared. The new hetera[2n]metacyclophanes obtained contain a benzophenone moiety as photoactive component. Although both forms possess identical building blocks and differ only in r

Preparation of polyfunctional arylmagnesium, arylzinc, and benzylic zinc reagents by using magnesium in the presence of LiCl

The presence of LiCl considerably facilitates the insertion of magnesium into various aromatic and heterocyclic bromides. Several functional groups, such as -OBoc, -OTs, -Cl, -F, -CF3, -OMe, -NMe2, and -N 2NR2, are well tolerated. The presence of a cyano group leads in some cases to competitive reduction of the organic halide to the corresponding ArH compound. The presence of sensitive groups such as methyl or ethyl ester is tolerated upon in situ trapping of the intermediate magnesium reagent with ZnCl2. This method can also be applied to the preparation of functionalized benzylic zinc reagents from benzylic chlorides. In the case of di- or tribromoaryl derivatives, directing groups such as -OPiv, -OTs, -N2NR2, or -OAc orient the zinc insertion (Zn/LiCl) to the ortho-position, while the reaction with Mg/LiCl or Mg/LiCl/ZnCl 2 leads to regioselective insertion into the para-carbon-bromine bond. Large-scale experiments (20-100 mmol) for all of the metalation procedures are described.