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(S)-2,5-Dihydro-1H-pyrrol-2-carbonsure

3,4-Dehydro-L-proline Struktur
4043-88-3
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( 148)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Capot Chemical Co.,Ltd.
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CHINA 722 55
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+undefined-21-51877795
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Alchem Pharmtech,Inc.
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CONIER CHEM AND PHARMA LIMITED
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Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34553 58

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
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