Isopropenylboronic Acidum Pinacol Ester CAS 126726-62-3 Purity >99.0% (GC) Factory High Quality

Description:

Nomen chemica: Isopropenylboronic Acidum Pinacol Ester

CAS: 126726-62-3

Puritas: >99.0% (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 chemica: Isopropenylboronic Acidum Pinacol Ester
CAS: 126726-62-3

Chemical Properties:

Nomen chemicum Isopropenylboronic Acidum Pinacol Ester
Synonyma 4,4,5,5-tetramethyl-2-(prop 1-en-2-yl) -1,3,2-dioxaborolane;2-(1-Methylethenyl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolanum
CAS Number 126726-62-3
CATTUS Number RF-PI1395
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C9H17BO2
M. Pondus 168.04
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Hyalina ad Pallida Liquid
Puritas / Analysis Methodus >99.0% (GC)
Humor (KF) ≤0.50%
Totalis immunditias <1.00%
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:

Isopropenylboronicum acidum Pinacol Ester (CAS: 126726-62-3) est versatile ester reagens usus ad palladium catalysatum Suzuki-Miyaura processuum transversim copulationum, electronico postulatio Diels-Alder reactionis inversae, cyclopropanationis Simmons-Smith, cycliationis polyenae; motus aldol stereoselectivae, Grubbs reactionem crucis-metathesis, reactionem intramolecularem Suzuki-Miyaura, transversim metathesis stereoselectivam, cycloadditionem dipolarem, iodosulfonylationem, asymmetricam additionem et hydroacylationem intramolecularem et praeparationem variarum kinasis therapeuticae et enzymaticae inhibitores.Isopropenylboronic acidum Pinacol Ester adhiberi potest ut medium in synthesi varietatis compositorum cyclicorum et acyclicorum organicorum.Ostenditur etiam α-Substitutum Allyl/Croty huius compositionis adhiberi posse pro valde Diastereo et Enantioselectivo allylboratione aldehydes.

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