(S)-(-)-tert-Butylsulfinamide CAS 343338-28-3 Puritas ≥99.0% ee≥99.0% Manufacturer Alta Puritas

Description:

Chemical Name: (S)-(-)-tert-Butylsulfinamide (S-BSN)

CAS: 343338-28-3

Aspectus: Alba ad Off-White pulveris

Puritas (LC): ≥99.0%

EE (LC): ≥99.0%

Chiral Compounds, High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com

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Product Detail

Product Tags

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	(S)-(-)-tert-Butylsulfinamide
Synonyma	(S)-(-)-2-Methyl-2-Propanesulfinamide;S-BSN
CAS Number	343338-28-3
CATTUS Number	RF-CC219
Stock Status	In Stock, Productio Ascendite ad Tons
Formulae hypotheticae	C4H11NOS
M. Pondus	121.2
Liquescens punctum	97.0~101.0℃
Solubilitas	Solutum in Methanol
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Aspectus	Alba ad Off-White pulveris
Imprimis Rotationes	-2.5° ~ -6.5° (C=1, CHCl3).
Puritas (LC)	≥99.0%
EE (LC)	≥99.0%
Totalis immunditias	≤1.0%
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:

FAQ:

Applicatio:

Shanghai Ruifu Chemical Co., Ltd. est primarium fabricae et supplementi (S)-(-)-tert-Butylsulfinamidei (CAS: 343338-28-3) cum qualitate magna, late in synthesi organica, synthesi intermedia et pharmaceutica Activa 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.

(S)-(-)-tert-Butylsulfinamide (CAS: 343338-28-3) adhibetur in reactione Suzuki.Usurpatur etiam pro reagens ad amines chirales componendos.Agit ut auxilia chiralis adhibita in synthesi asymmetrica trifluoroethylaminarum per conversionem trifluoroacetaldisi ad imina chiralis.Involvitur etiam in transformatione P,N-sulfinyl ligandi imine per condensationem cum aldehydis et ketonibus, quae iridium catalysatum asymmetricum hydrogenii olefinorum subire possunt.Praeterea, gerens est ad intermedia pharmaceutica et pharmaceutica conficienda.