Allylboronic Acidum Pinacol Ester CAS 72824-04-5 Purity > 98.0% (GC) Factory High Quality

Description:

Nomen chemicum: Allylboronic Acidum Pinacol Ester

CAS: 72824-04-5

Puritas: >98.0% (GC)

Aspectus: Hyalina ad Pallida Liquid

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Descriptio:

Manufacturer Supple Quality, Commercial Productio
Nomen chemicum: Allylboronic Acidum Pinacol Ester CAS: 72824-04-5

Chemical Properties:

Nomen chemicum Allylboronic Acidum Pinacol Ester (confirmatur cum Phenothiazine)
Synonyma 2-Allyl-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane;2-(Prop-2-en-1-yl) -4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane.
CAS Number 72824-04-5
CATTUS Number RF-PI1390
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C9H17BO2
M. Pondus 168.04
Ferveret 50.0~53.0℃/5 mmHg (lit.)
Density 0.896 g/ml ad 25℃ (lit.)
Index refractivus (N20/D) 1.425~1.427
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Hyalina ad Pallida Liquid
Puritas / Analysis Methodus >98.0% (GC)
Confirmatur cum Phenothiazine <2.00%
Totalis immunditias <2.00%
Test Standard Enterprise Standard
Consuetudinem Pharmaceutical intermedia

Sarcina & Repono:

sarcina: Utrem, 25kg/ferrum, vel secundum exigentiam emptoris.

Repono Condition:Repone in vasis signatis in loco frigido et sicco;A luce et humore protege.

commoda:

1

FAQ:

Applicatio:

Allylboronicum acidum Pinacol Ester (CAS: 72824-04-5) agere potest ut reagens adhibita pro Palladio catalysed Suzuki-Miyaura-coniunctio et metathesis olefina;Additiones radicales intermoleculares;Allylboratio aldehydes catalysata per diolum spirobiindanum chiralum (SPINOL) innititur acida phosphorica et hydrovinyla- tionis regioselectivae cum alkenibus cobalt-catalysis;Acidum nuclei temptatum translatio ducens ad reactionem photorelease et stereoselectivam indium-catalyticum motus Hosomi-Sakurai.Allylboronicum acidum Pinacol Ester reagit cum acida carboxylicis, coram hydride tri-n-butyltin, ut alcoholos homoallylicos in bono cedat dare.Alcoholi homoallylici etiam per allylborationem aldehydarum formari possunt.

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