PCC Pyridinium Chlorochromate CAS 26299-14-9 Intende ≥98.5% Factory

Description:

Nomen chemicum: Pyridinium Chlorochromate

Synonyma: PCC

CAS: 26299-14-9

Dic: ≥98.5%

Aspectus: Aliquam ut lux Brown pulveris

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Descriptio:

Manufacturer Supple, Puritas, Commercial Productio
Nomen chemicum: Pyridinium Chlorochromate (PCC)
CAS: 26299-14-9

Chemical Properties:

Nomen chemicum Pyridinium Chlorochromatum
Synonyma PCC
CAS Number 26299-14-9
CATTUS Number RF-PI535
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C5H6N·ClCrO3
M. Pondus 215.55
Liquescens punctum 205.0 ad 208.0℃ (lit.)
Solubilitas Solutum in Acetone, Benzene, Dichloromethane, Acetonitrile
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Orange crystallinum pulveris
Assay ≥98.5%
Damnum in Siccatio ≤1.0%
Metalla gravia (ut Pb) ≤20ppm
Test Standard Enterprise Standard
Consuetudinem Oxidizing agentis

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:

Pyridinium Dichromate (PDC) vel Pyridinium Chlorochromate (PCC) in mediis anhydrois sicut dichloromethanum oxidizat alcoholos primarios ad aldehydes, vitando superoxidationem ad acida carboxylica.PCC primum nova oxidantis selectiva ab EJ Corey anno 1975 inventa, postquam investigationem enucleavit.Reagens est in synthesi organica adhibita principaliter pro oxidatione alcoholorum ad carbonyls formandos.Varietas compositionum affinium cum simili reactivitate cognoscitur.PCC commodum oxidationis selectivae alcoholorum praebet ad aldehydes vel ketones, cum multa alia reagentia minus selectiva sunt.Pyridinium Chlorochromate adhibetur pro agente oxidizing ad alcoholos primas et secundas convertendas ad aldehydes et ketones respective.In praeparatione cyclohexanonis, pulegonis et lactones implicatur.Magni ponderis munus agit in mono-oxidatione xylenum selectivae ad tolualdehydes et arylhydroxyamines ad compositorum nitrosorum.Praeterea adiuvatur ut oxidant pro amino acidis, cystinis, anilinis, cycloalkanolis, vicinalibus et non-vicinalibus diolis ac in reactione oxidationis Bablerae.

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