Carboxyphenylboronic Acidum CAS 14047-29-1 Puritas >99.5% (HPLC) Factory Top Quality

Description:

Nomen chemicum: 4-Carboxyphenylboronic Acid

CAS: 14047-29-1

Puritas: >99.5% (HPLC)

Aspectus: pulveris albi

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Descriptio:

Manufacturer Supple Quality, Commercial Productio
Nomen chemicum: 4-Carboxyphenylboronic Acidum CAS: 14047-29-1

Chemical Properties:

Nomen chemicum Carboxyphenylboronic Acidum 4-(Contains variae copiae anhydrid)
Synonyma 4-Carboxybenzeneboronic Acidum
CAS Number 14047-29-1
CATTUS Number RF-PI1293
Stock Status In Stock, Productio Ascendite usque ad XXV Tons / Mensis
Formulae hypotheticae C7H7BO4
M. Pondus 165.94
Liquescens punctum 220℃ (decl.)
Solubilitas Solutum in Methanol
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Alba pulveris
Puritas / Analysis Methodus >99.5% (HPLC)
Damnum in Siccatio <0.50%
Residere in Ignition <0.20%
una immunditia <0.50%
Totalis immunditias <0.50%
Metalla gravia (ut Pb) <20ppm
Test Standard Enterprise Standard
Consuetudinem Pharmaceutical intermedia

Sarcina & Repono:

sarcina: Utrem, aluminium foil, sacculum, 25kg/cardboard Drum, vel secundum exigentiam emptoris.

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

commoda:

1

FAQ:

Applicatio:

4-Acidum carboxyphenylboricum (CAS: 14047-29-1) valde versatile reagens est.Reagens usus est in variis reactionibus inclusis cum condensatione reactiones stabilientium catenis in superficie polystyrene latex, motus coniunctionis Suzuki, esterificationis, derivationis polyvinylamine.Reagentia usus est ad Suzuki-Miyaura crucis-coniunctionem, inductionem pH sensibilitatis in fluorescentiae vita quantis punctis a tincturis fluorescentibus NIR, bio-sustentatis palladium nanoparticularum sicut phosphinum liberum catalystum propter reactionem in aqua et Chan-Lam-type Copper ( Cu)catalyzum S-arylation cum arylis acida boronicis ad locus temperatus.Reagentia adhibita est ad parandum isoquinolonum per regioselectivam Suzuki-Miyaura-coniugationem et tandem palladium catalysatum intramolecularem aminocarbonylationem et annulationem.

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