(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure
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
(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
Wasserl?slichkeit
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-S?tze:
22-24/25
WGK Germany
3
RTECS-Nr.
UX9371345
HS Code
2933.99.9701
(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure Chemische Eigenschaften,Einsatz,Produktion Methoden
S-S?tze 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 H?ndler.
Global( 150)Lieferanten
Americas 1
China 93
Europe 1
Germany 5
India 3
Japan 3
Switzerland 2
The Netherlands 1
United Kingdom 5
United States 36
Global 150
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