468751-38-4

Basic information

• Product Name: 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE
• Synonyms: 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE;2-(BENZENESULFONYLMETHYL)BENZALDEHYDE;2-FORMYLBENZYL PHENYL SULFONE;2-(Benzenesulfonylmethyl)benzaldehyde 2-Formylbenzyl Phenyl Sulfone
• CAS NO: 468751-38-4
• Molecular Formula: C₁₄H₁₂O₃S
• Molecular Weight: 260.31
• Mol File: 468751-38-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: 141.0 to 145.0 °C
• Boiling Point: 480.8 °C at 760 mmHg
• Flash Point: 313.3 °C
• Appearance: /
• Density: 1.278 g/cm³
• Vapor Pressure: 2.11E-09mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE(468751-38-4)
• EPA Substance Registry System: 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE(468751-38-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 468751-38-4(Hazardous Substances Data)

Usage

General Description

2-(Phenylsulfonylmethyl)benzaldehyde is a chemical compound with the molecular formula C15H14O2S. It is a benzaldehyde derivative with a phenylsulfonylmethyl group attached to the benzene ring. 2-(PHENYLSULFONYLMETHYL)BENZALDEHYDE is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is also used as a reagent in chemical reactions for the introduction of the phenylsulfonylmethyl group into other compounds. Additionally, it has potential applications in the development of new materials and in medicinal chemistry due to its unique structure and reactivity.

InChI:InChI=1/C14H12O3S/c15-10-12-6-4-5-7-13(12)11-18(16,17)14-8-2-1-3-9-14/h1-10H,11H2

Upstream product

• 873-55-2 sodium benzenesulfonate 
• 22115-41-9 2-(bromomethyl)benzonitrile 
• 2042-37-7 o-cyanobromobenzene 
• 618-41-7 Benzenesulfinic acid 
• 529-19-1 2-Methylbenzonitrile 
• 184176-33-8 methyl o-[α-phenylsulfonyl]toluate 
• 300396-14-9 2-[(benzenesulfonyl)methyl]benzoic acid 
• 89-71-4 2-Methyl-benzoic acid methyl ester 
• 2417-73-4 methyl 2-bromomethylbenzoate 
• 911836-71-0 C₁₄H₁₄O₃S 
• 82651-72-7 ortho-(phenylsulfonylmethyl)benzonitrile 

Downstream Products

• 226089-80-1 2-(2-benzenesulfonylmethyl-phenyl)-[1,3]dioxolane 
• 53397-65-2 sym-dibenzo-1,5-cyclooctadiene-3,7-diyne 
• 468751-39-5 5,11-bis-benzenesulfonyl-dibenzo[a,e]cyclooctene 
• 53223-75-9 12H-dibenzo[b,h]fluoren-12-one 
• 468751-39-5 5,11-bis(phenylsulfonyl)dibenzo[a,e][8]annulene 
• 1253203-72-3 1,8-dibenzyl-1,8-dihydrodibenzo[3,4:7,8]cycloocta[1,2-d:5,6-d']bis([1,2,3]triazole) 
• 1253203-73-4 C₃₀H₂₂N₆ 
• 1388113-86-7 C₅₂H₅₈O₂ 
• 1388113-81-2 C₃₂H₁₈ 
• 1388114-08-6 C₅₀H₄₁BrO 
• 1388114-05-3 C₈₄H₇₄O₂ 
• 1388114-04-2 C₆₈H₆₆O₂ 
• 1388114-03-1 C₃₄H₃₃BrO 
• 1388114-00-8 C₄₃H₂₆N₂ 

Relevant articles and documents

A visible-light photoactivatable di-nuclear PtIV triazolato azido complex

A novel PtIV triazolato azido complex [3]-[N1,N3] has been synthesised via a strain-promoted double-click reaction (SPDC) between a PtIV azido complex (1) and the Sondheimer diyne (2). Photoactivation of [3]-[N1,N3] with visible ligh

Cyclopropenone-caged Sondheimer diyne (dibenzo[a,e]cyclooctadiyne): A photoactivatable linchpin for efficient SPAAC crosslinking

The first fully conjugated bis-cyclopropenone (photo-DIBOD), a derivative of dibenzo[a,e][8]annulene, has been synthesized. 350-420 nm irradiation of this robust compound results in the efficient formation of dibenzo [a,e] cyclooctadiyne, an unstable, but

Regiospecific synthesis of benzo[b]fluorenones via ring contraction by benzil-benzilic acid rearrangement of benz[a]anthracene-5,6-diones

A regiospecific route to benzo[b]fluorenones is described. The synthesis is based upon a one-pot, regiospecific benzannulation of 1,4-dipolar synthons with naphthoquinone monoketal and ring contraction of the generated benz[a]anthracene-5,6-diones through benzil-benzilic acid rearrangement. Georg Thieme Verlag Stuttgart.