(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure
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- CAS-Nr.
- 4043-88-3
- Bezeichnung:
- (S)-2,5-Dihydro-1H-pyrrol-2-carbonsure
- Englisch Name:
- 3,4-Dehydro-L-proline
- Synonyma:
- 3,4-DEHYDRO-L-PROLINE HYDROCHLORIDE;Dehydro L;H-DELTA-PRO-OH;H-dehydro-Pro-OH;H-DEHYDROPRO-OH HCL;3,4-DEHYDRO-PROLINE;3,4-Didehydroproline;3,4-Dehydro-L-Pro-OH;l-3,4-dehydroproline;H-3,4-DEHYDRO-PRO-OH
- CBNumber:
- CB8128986
- Summenformel:
- C5H7NO2
- Molgewicht:
- 113.11
- MOL-Datei:
- 4043-88-3.mol
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(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure Eigenschaften
- Schmelzpunkt:
- 239-241 °C (dec.)
- Siedepunkt:
- 211.82°C (rough estimate)
- Dichte
- 1.2416 (rough estimate)
- Brechungsindex
- 1.4200 (estimate)
- storage temp.
- Sealed in dry,2-8°C
- Wasserlöslichkeit
- Soluble in water
- Aggregatzustand
- powder to crystal
- pka
- 2.04±0.20(Predicted)
- Farbe
- White to Amber to Dark green
- BRN
- 5376764
- CAS Datenbank
- 4043-88-3(CAS DataBase Reference)
Sicherheit
| S-Sätze: |
22-24/25 |
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| WGK Germany |
3 |
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| RTECS-Nr. |
UX9371345 |
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| HS Code |
2933.99.9701 |
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(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure Chemische Eigenschaften,Einsatz,Produktion Methoden
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
Crystalline
Verwenden
3,4-Dehydro-L-proline is used to prepare morpholinyl-4-piperidinylacetic acid derivatives as potent oral active VLA-4 antagonist. It is also a β-Proline analog used as agonists at the strychnine-sensitive glycine receptor.
(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 142)Lieferanten
4043-88-3((S)-2,5-Dihydro-1H-pyrrol-2-carbonsure)Verwandte Suche:
- (s)-2,5-dihydro-1h-pyrrole-2-carboxylicacid
- 5-dihydro-(s)-1h-pyrrole-2-carboxylicaci
- 3,4- Dehydro-L-proline, (S)-3-Pyrroline-2-carboxylic acid
- (S)-3,4-Dehydro-pyrrolidine-2-carboxylic acid
- 3,4-Dehydro-L-proline99+%
- 3,4-Dehydro-L-Pro-OH
- 3,4-DEHYDRO-L -PROLINE CRYSTALLINE
- (S)-3-Pyrroline-2-carboxylic acid, 3,4-Didehydro-L-proline
- 3,4-Didehydroproline
- (2S)-2,5-dihydro-1H-pyrrole-2-carboxylic acid
- (2S)-3-pyrroline-2-carboxylic acid
- l-3,4-dehydroproline
- l-3-pyrroline-2-carboxylicaci
- H-3,4-DEHYDRO-PRO-OH
- H-DEHYDROPRO-OH HCL
- H-DELTA-PRO-OH
- H-PRO(3,4-DEHYDRO)-OH
- (S)-2,5-DIHYDROPYRROLE-2-CARBOXYLIC ACID
- (S)-3-PYRROLINE-2-CARBOXYLIC ACID
- 3,4-DIDEHYDRO-L-PROLINE
- 3,4-DEHYDRO-L-PROLINE
- 3,4-DEHYDRO-PROLINE
- 3,4-DEHYDRO-PRO-OH HCL
- Dehydro L
- 3,4-Dehydro-L-proline>
- H-dehydro-Pro-OH
- 1H-Pyrrole-2-carboxylic acid, 2,5-dihydro-, (2S)-
- (S)-3-Pyrroline-2-carboxylicAci
- 3,4-Dehydro-L-proline USP/EP/BP
- 3,4-dehydro-laevo-proline
- 3,4-DEHYDRO-L-PROLINE HYDROCHLORIDE
- Prinomastat Impurity 3
- 4043-88-3
- Biochemicals and Reagents
- BioChemical
- Specialty Synthesis
- Proline Derivatives
- Peptide Synthesis
- Substrate Analogs
- Unnatural Amino Acid Derivatives
- Enzymes, Inhibitors, and Substrates
- Enzyme Inhibitors by Type
- Enzyme Inhibitors
- Chiral Compound
- Amino Acids
