4-Aminophenylboronic Acidum Pinacol Ester CAS 214360-73-3 Purity >99.0% (GC) Factory High Quality

Description:

Nomen chemicum: 4-Aminophenylboronic Acidum Pinacol Ester

CAS: 214360-73-3

Puritas: >99.0% (GC)

Aspectus: Yellow ad Reddish-brunneis solidus

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Descriptio:

Manufacturer Supple Quality, Commercial Productio
Nomen: 4-Aminophenylboronic Acidum Pinacol EsterCAS: 214360-73-3

Chemical Properties:

Nomen chemicum 4-Aminophenylboronic Acidum Pinacol Ester
Synonyma 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline;2-(4-Aminophenyl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolanum
CAS Number 214360-73-3
CATTUS Number RF-PI1274
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C12H18BNO2
M. Pondus 219.09
Solubilitas in Hot Methanol Prope diaphanum
Solubilitas in aqua Insolubilis in aqua
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Flavo ad rufo-brunneis solidus
Puritas / Analysis Methodus >99.0% (GC)
Liquescens punctum 166.0~170.0℃
Aqua (auctore Karl Fischer) <0.30%
Totalis immunditias <1.00%
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-Aminophenylboronic Acidum Pinacol Ester (CAS: 214360-73-3) ut medium adhibetur in synthesi organica et industria pharmaceutica et materiae ducatur.Potest adhiberi ut reagens ad Crucis Suzuki-Miyaura coitus reactionem.Acidum aryl boricum late adhiberi potest ut tutus et environmentally- amica novus aryl gerens in pharmaceuticis, pesticidis, materiis provectis et aliis subtilibus chemicis, quae structuram aryl investigationis et productionis continentur.Reactio inter acidum arylboricum et halogenatum magni ponderis munus agit in synthesi medicamento hodierno.Hoc genus reactionis a Suzuki team, physico Iaponico propositus est, et Praemium Nobelianum in Chemia anno 2010 vicit.

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