(R)-(+)-1,1′-Bi-2-naphthol CAS 18531-94-7 Intende ≥99.5% (HPLC) ee≥99.5% Alta Puritas

Description:

Nomen chemicum: (R)-(+)-1,1′-Bi-2-naphthol

Synonyma: (R) -(+) -BINOL

CAS: 18531-94-7

Aspectus: Crystallinus Powder Alba

Chiral Asssay: ee ≥99.5% (HPLC) Columna Chiral

Chemical Asssay: ≥99.5% (HPLC)

Chiral Compounds, High Quality, Commercial Production


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Descriptio:

Chemical Properties:

Nomen chemicum (R)-(+)-1,1'-Bi-2-naphthol
Synonyma (R)-(+)-BINOL
CAS Number 18531-94-7
CATTUS Number RF-CC216
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C20H14O2
M. Pondus 286.32
Density 1.301
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Crystallina pulveris alba
Damnum in Siccatio ≤0.50%
Liquescens punctum 208.0~210.0℃
Imprimis Rotationes [a]22/D +34.0° ~ +37.0° (C=1 in THF)
Chiral Asssay ee ≥99.5% (HPLC) Chiral Column
Chemical Asssay ≥99.5% (HPLC)
Test Standard Enterprise Standard
Consuetudinem Chiral Compositions;Pharmaceutical intermedia

Sarcina & Repono:

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

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine, humore et pestis infestatione.

commoda:

1

FAQ:

Applicatio:

Shanghai Ruifu Chemical Co., Ltd. est primarius fabricae et supplementi (R)-(+)-1'-Bi-2-naphthol (CAS: 18531-94-7) magna qualitate, late organicis adhibitis. synthesis, synthesis intermediorum pharmaceuticorum et synthesis chemicae tenuis.

Shanghai Ruifu Chemical Co, Ltd. magni ponderis munus agit in chymiae chiralae, societas commissa productioni compositionum chiralium.Nostri fructus a clientibus late laudantur.

(R)-(+)-1,1'-Bi-2-NAPHTHOL (CAS: 18531-94-7) fit per resolutionem BINOL racemici, quod fieri solet ex 2-naphthol chloride catalyzis ferreis (III) per reactionem radicitus.(R)-(+)-1,1'-Bi-2-naphtholum in variis applicationibus late adhibitum: 1) agentium chiralium inducentium pro catalyticis, asymmetricis reactiones sicut Diels-Alder reactionem, seu reactionem, seu sicut Lewisacidas ;2) reductio enantioselectiva ketonum;3) Synthesis chiralis macrocycles et alia cura compositorum.Binapthol imminium sal praecursoris chiralis adhibita in oxidatione asymmetrica catalytica sulfidelium ad sulfoxides.Chiral lanthanidei triflationes ex binaphthol formatae inserviunt catalysts pro reactionibus asymmetricis Diels-Alder.Derivationes binaphtoli nuper adhibitae sunt in conversionibus asymmetricis Claisen et epoxidationibus asymmetricis.Lithium aluminii hydride derivativa harum diolarum (BINAP-H) late adhibita est ad reductionem ketonum.In praeparatione biosynthetica adhibetur pro oxidatione enantioselectiva naphtholti ad binaphthyldiola cum peroxidase catalyst equiradico.

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