Sie suchten nach: Ethyl+1-benzyl-4-oxopiperidine-3-carboxylate+hydrochloride

87'068 results were found

Suchergebnis einschränken: Sortieren nach

Sort Results

Listenansicht Easy View

Vergleichen(0) Entfernen

Bewerten Sie das Suchergebnis

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid Crosslinker

Lieferant: G-Biosciences

Beschreibung: EDC is a heterobifunctional, water-soluble, zero-length carbodiimide crosslinker that is used to couple carboxyl groups to primary amines. EDC activates carboxyl groups first and forms amine reactive O-acylisourea imtermediate that spontaneously reacts with primary amines to form an amide bond and isourea by-product.

(S)-2-Piperidinone-6-carboxylic acid 98%

Artikel-Nr: (APOSOR51818-1G)

Lieferant: Apollo Scientific

Hersteller Artikel Nummer : OR51818-1G

Beschreibung: (S)-2-Piperidinone-6-carboxylic acid 98%

UOM: 1 * 1 g

Sale

N/A Each

trans-2,6-Dimethylpiperidin-4-one, N-BOC protected

Lieferant: Apollo Scientific

Beschreibung: trans-2,6-Dimethylpiperidin-4-one, N-BOC protected

1-Boc-3-fluoro-4-piperidone 96%

Lieferant: Apollo Scientific

Beschreibung: 1-Boc-3-fluoro-4-piperidone 96%

1-Boc-3-fluoro-4-piperidone 97%

Lieferant: Thermo Fisher Scientific

Beschreibung: 1-Boc-3-fluoro-4-piperidone 97%

Sicherheitsdatenblätter

Nicardipin -hydrochlorid, gelb, fest

Artikel-Nr: (PROOTRCN394500-50)

Lieferant: LGC Standards PROMOCHEM

Hersteller Artikel Nummer : TRCN394500-50

Beschreibung: Nicardipin -hydrochlorid, gelb, fest

UOM: 1 * 50 mg

Sale

N/A Each

(R)-Ethyl-3-piperidincarboxylat Hydrochlorid

Lieferant: ACTIVATE SCIENTIFIC

Beschreibung: (R)-Ethyl-3-piperidincarboxylat Hydrochlorid

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid, No-Weigh™, Pierce™

Artikel-Nr: (PIERA35391)

Lieferant: Thermo Fisher Scientific

Hersteller Artikel Nummer : A35391

Beschreibung: Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

UOM: 1 * 10 mg

Sale