(R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Puritas ≥99.0% ee≥99.0% Manufacturer Alta Puritas

Description:

Nomen chemicum: (R)-(+)-tert-Butylsulfinamide (R-BSN)

CAS: 196929-78-9

Aspectus: Alba ad Off-White pulveris

Puritas (LC-220um): ≥99.0%

EE (LC): ≥99.0%

Chiral Compounds, High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com  


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Descriptio:

Manufacturer Supple cum High puritate et stabulo Quality
(R)-(+)-tert-Butylsulfinamide CAS 196929-78-9
(S)-(-)-tert-Butylsulfinamide CAS 343338-28-3
Chiral Compounds, High Quality, Commercial Production

Chemical Properties:

Nomen chemicum (R)-(+)-tert-Butylsulfinamide
Synonyma (R)-(+)-2-Methyl-2-Propanesulfinamide;R-BSN
CAS Number 196929-78-9
CATTUS Number RF-CC218
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C4H11NOS
M. Pondus 121.2
Liquescens punctum 103.0~ 107.0℃
Solubilitas Solutum in Methanol
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Alba ad Off-White pulveris
Puritas (LC-220nm) ≥99.0%
EE (LC) ≥99.0%
Imprimis Rotationes +2.5° ~ +6.5° (C=1, CHCl3).
una immunditia ≤0.50%
Totalis immunditias <1.00%
Metalla gravia (ut Pb) <20ppm
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 primarium fabricae et supplementi (R)-(+)-tert-Butylsulfinamidei (CAS: 196929-78-9) magna qualitate, late in synthesi organica, synthesi intermedia et pharmaceutica Active Pharmaceutical Ingrediens (API) synthesis

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

(R)-(+)-2-Methyl-2-propanesulfinamide ligandum chirale est, quod in compositionibus pharmaceuticis adhibetur.Ad praeparationem sulfinamides beta-chloro adhibetur in synthesi chiralorum azridinarum.In praeparatione organocatalysi ad enantioselectivam iminum reductionem implicatur.Hoc gerens est ad aminas chiralis componendas.Praeter hoc, in P,N-sulfinyl ligandum imine convertitur per condensationem cum aldehydibus et ketonibus quae iridium catalysatum asymmetricum hydrogenii olefins sustinent.

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