N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE
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- 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 98%
- CBNumber:
- CB0153429
- Summenformel:
- C12H22N2O4
- Molgewicht:
- 258.31
- MOL-Datei:
- 115186-37-3.mol
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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 Rotation
- [α]22/D 38°, c = 1 in methanol
- Major Application
- peptide synthesis
- InChI
- 1S/C12H22N2O4/c1-12(2,3)18-11(16)14-8-6-7-9(14)10(15)13(4)17-5/h9H,6-8H2,1-5H3/t9-/m0/s1
- InChIKey
- KPVRHJIGNMLCHG-VIFPVBQESA-N
- SMILES
- CON(C)C(=O)[C@@H]1CCCN1C(=O)OC(C)(C)C
Sicherheit
| WGK Germany |
3 |
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| HS Code |
2933998090 |
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| Speicherklasse |
10 - Combustible liquids |
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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
N-(TERT-BUTOXYCARBONYL)-L-PROLINE N'-METHOXY-N'-METHYLAMIDE Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 70)Lieferanten
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
- N-(tert-Butoxycarbonyl)-L-proline N′-methoxy-N′-methylamide, CAS 115186-37-3
- tert-Butyl (S)-2-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate
- 115186-37-3
- Amino Acid Derivatives
- Peptide Synthesis
- Specialty Synthesis
- Amino Acid Derivatives
- Peptide Synthesis
- Proline
- Amino Acids
