27096-64-6

Basic information

• Product Name: AKOS BBB/400
• Synonyms: ASINEX-REAG BAS 00724393;CHEMBRDG-BB 4023578;AKOS BBB/400;TIMTEC-BB SBB010317;UKRORGSYN-BB BBV-182192;2-(allyloxy)aniline(SALTDATA: HCl);2-prop-2-enoxyaniline;2-(allyloxy)benzenamine
• CAS NO: 27096-64-6
• Molecular Formula: C₉H₁₁NO
• Molecular Weight: 149.19
• Mol File: 27096-64-6.mol
• Article Data: 31

Chemical Properties

• Boiling Point: 258.3°C at 760 mmHg
• Flash Point: 116°C
• Appearance: /
• Density: 1.037g/cm³
• Vapor Pressure: 0.0138mmHg at 25°C
• Refractive Index: 1.554
• PKA: 4.48±0.10(Predicted)
• CAS DataBase Reference: AKOS BBB/400(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS BBB/400(27096-64-6)
• EPA Substance Registry System: AKOS BBB/400(27096-64-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 27096-64-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H11NO/c1-2-7-11-9-6-4-3-5-8(9)10/h2-6H,1,7,10H2

Upstream product

• 55339-51-0 2-allyloxy-1-nitrobenzene 
• 1746-13-0 allyl phenyl ether 
• 186663-74-1 tert-butyl (2-hydroxyphenyl)carbamate 
• 24892-63-5 1-allyloxy-2-iodobenzene 
• 106-95-6 allyl bromide 
• 95-55-6 2-amino-phenol 
• 6622-73-7 4-acetamidophenyl allyl ether 
• 88-75-5 2-hydroxynitrobenzene 
• 1624-53-9 2-(benzylideneamino)phenol 
• 55000-07-2 o-(prop-2-enyloxy)phenyl azide 
• 614-80-2 2-(acetylamino)phenol 
• 91132-57-9 2-Acetylamino-phenyl-allyl-ether 

Downstream Products

• 61364-10-1 chloro-(2-allyloxy-phenylhydrazono)-acetic acid ethyl ester 
• 107195-52-8 2-(2'-Allyloxyanilino)-2-phenylessigsaeure-ethylester 
• 128255-33-4 1-Allyloxy-2-isocyanato-benzene 
• 78480-09-8 o-<<(Z)-1-Propenyl>oxy>aniline 
• 100619-01-0 N_.N-Bis-(2-hydroxy-aethyl)-2-allyloxy-anilin 
• 25125-40-0 1-(2-(allyloxy)phenyl)-2-(tetrafluoro-λ⁵-boraneyl)diazene 
• 65461-42-9 4-Allyl-2-amino-phenol 
• 103200-16-4 N-(2-(allyloxy)phenyl)formamide 
• 911023-30-8 2-(allyloxy)-N-(tert-butoxycarbonyl)formanilide 
• 911023-32-0 (2-allyloxy-phenyl)-vinyl-carbamic acid tert-butyl ester 
• 113002-45-2 (E)-3-(2,3-dihydrobenzofuran-3-yl)-1-phenylpropene 
• 1446029-14-6 [2-(allyloxy)phenyl](phenyl)selane 
• 21535-97-7 3-methyl-benzofuran 
• 111191-89-0 3-<(selenophenyl)methyl>-2,3-dihydrobenzofuran 

Relevant articles and documents

Copper-catalyzed three-component reaction of arylhydrazine hydrochloride, DABSO, and NFSI for the synthesis of arenesulfonyl fluorides

This paper reports a convenient copper-catalyzed three-component conversion of arylhydrazine hydrochlorides to arenesulfonyl fluorides in good yields under mild conditions, using 1,4-diazabicyclo [2.2.2]octane bis(sulfur dioxide) (DABSO) as a sulfonyl source andN-fluorobenzenesulfonimide (NFSI) as a fluorine source based on a radical sulfur dioxide insertion and fluorination strategy. Notably, arylhydrazine hydrochloride is used as a safe precursor of aryl radicals.

Copper-free Sandmeyer-type Reaction for the Synthesis of Sulfonyl Fluorides

A copper-free Sandmeyer-type fluorosulfonylation reaction is reported. Utilizing Na2S2O5 and Selectfluor as the sulfur dioxide and fluorine sources, respectively, aryldiazonium salts were transformed into sulfonyl fluorides. The one-pot direct synthesis of sulfonyl fluorides from aromatic amines was also realized via in situ diazotization. The practicality of this method was demonstrated by the broad functional group tolerance, gram-scale synthesis, and late-stage fluorosulfonylation of natural products and pharmaceuticals.

Intramolecular Aminoazidation of Unactivated Terminal Alkenes by Palladium-Catalyzed Reactions with Hydrogen Peroxide as the Oxidant

The palladium-catalyzed aminoazidation of aminoalkenes yielding azidomethyl-substituted nitrogen-containing heterocycles was developed. The procedure requires oxidative conditions and occurs at room temperature in the presence of hydrogen peroxide and NaN3 as the azide source. These conditions provide selective exo-cyclization/azidation of the carbon-carbon double bond, furnishing a versatile approach toward five-, six-, and seven-membered heterocyclic rings.