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N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE

N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Struktur
115186-37-3
CAS-Nr.
115186-37-3
Englisch Name:
N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
Synonyma:
BOC-PRO-N(OME)ME;BOC-PRO-NME(OME);Boc-L-Pro-N(OMe)Me;BOC-L-PROLINE N,O-DIMETHYL HYDROXAMIDE;N-(t-BOC)-L-proline-N'-methoxy-N'-methylamide;Boc-L-prolineN,O-dimethylhydroxamide≥ 95% (HPLC);(S)-1-Boc-2-[Methoxy(Methyl)carbaMoyl]pyrrolidine;N-(tert-butoxycarbonyl)-L-proline N'-methoxy-N'-M;N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE;N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
CBNumber:
CB0153429
Summenformel:
C12H22N2O4
Molgewicht:
258.31
MOL-Datei:
115186-37-3.mol

N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Eigenschaften

Siedepunkt:
253 °C(lit.)
Dichte
1.059 g/mL at 25 °C(lit.)
Brechungsindex
n20/D 1.471(lit.)
Flammpunkt:
113 °C
storage temp. 
Sealed in dry,2-8°C
pka
-3.38±0.40(Predicted)
Optische Aktivit?t
[α]22/D 38°, c = 1 in methanol

Sicherheit

WGK Germany  3
HS Code  2933998090

N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Light yellow liquid

Verwenden

α-Amino Weinreb amide.

N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

1-Propanone, 1-(2S)-2-pyrrolidinyl-

N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 62)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hangzhou FandaChem Co.,Ltd. 		+8615858145714
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CONIER CHEM AND PHARMA LIMITED 		+8618523575427
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Nextpeptide Inc 		+86-0571-81612335 +8613336028439
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Hefei TNJ Chemical Industry Co.,Ltd. 		+86-0551-65418684 +8618949823763
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115186-37-3()Verwandte Suche:

  • BOC-L-PROLINE N,O-DIMETHYL HYDROXAMIDE
  • BOC-PRO-NME(OME)
  • BOC-PRO-N(OME)ME
  • N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
  • N-(tert-butoxycarbonyl)-L-proline N'-methoxy-N'-M
  • N-(tert-Butoxycarbonyl)-L-proline N'-methoxy-N'-methylamide 98%
  • Boc-L-prolineN,O-dimethylhydroxamide≥ 95% (HPLC)
  • Boc-L-Pro-N(OMe)Me
  • (S)-tert-butyl 2-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate
  • Tert-butyl (2S)-2-{[methoxy(methyl)amino]carbonyl}pyrrolidine-1-carboxylate
  • (S)-1-Boc-2-[Methoxy(Methyl)carbaMoyl]pyrrolidine
  • tert-butyl (2S)-2-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylate
  • (S)-2-(N-Methoxy-N-methylcarbamoyl)pyrrolidine-1-carboxylic acid tert-butyl ester
  • 1-Pyrrolidinecarboxylic acid, 2-[(methoxymethylamino)carbonyl]-, 1,1-dimethylethyl ester, (2S)-
  • ert-butyl(2S)-2-[methoxy(methyl)carbamoyl]pyrrolidine-1-carboxylate
  • N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE USP/EP/BP
  • N-(t-BOC)-L-proline-N'-methoxy-N'-methylamide
  • N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
  • 115186-37-3
  • Amino Acid Derivatives
  • Peptide Synthesis
  • Specialty Synthesis
  • Amino Acid Derivatives
  • Peptide Synthesis
  • Proline
  • Amino Acids
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