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Casa. > prodotti > Intermediati farmaceutici > Fmoc-D-Aph(Cbm)-OH CAS 324017-22-3 with Molecular Formula C25H23N3O5 and Molecular Weight 445.47 for GnRH Antagonist Activity

Fmoc-D-Aph(Cbm)-OH CAS 324017-22-3 with Molecular Formula C25H23N3O5 and Molecular Weight 445.47 for GnRH Antagonist Activity

Dettagli del prodotto

Luogo di origine: Cina

Marca: Sunshine

Certificazione: ISO,COA

Numero di modello: 324017-22-3

Termini di pagamento e di spedizione

Quantità di ordine minimo: Negoziazione

Prezzo: negotiable

Imballaggi particolari: Sacca in alluminio, tamburo

Tempi di consegna: 7-15 giorni

Termini di pagamento: L/C, D/A, D/P, T/T, Western Union

Capacità di alimentazione: TONNELLATA

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Evidenziare:

CAS 324017-22-3 Fmoc-D-Aph(Cbm)-OH

,

Molecular Formula C25H23N3O5 Fmoc-D-Aph(Cbm)-OH

,

Molecular Weight 445.47 Fmoc-D-Aph(Cbm)-OH

CAS NO::
324017-22-3
Aspetto::
Solido bianco o quasi bianco
Formula molecolare::
C25H23N3O5
Peso molecolare::
445.47
Einecs no::
811-283-2
MDL NO.::
MFCD26743751
CAS NO::
324017-22-3
Aspetto::
Solido bianco o quasi bianco
Formula molecolare::
C25H23N3O5
Peso molecolare::
445.47
Einecs no::
811-283-2
MDL NO.::
MFCD26743751
Fmoc-D-Aph(Cbm)-OH CAS 324017-22-3 with Molecular Formula C25H23N3O5 and Molecular Weight 445.47 for GnRH Antagonist Activity

Product Description:
Fmoc-D-Aph(Cbm)-OH CAS 324017-22-3



Synonyms:
D-Phenylalanine, 4-[(aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-;
(2R)-3-[4-(carbamoylamino)phenyl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic Acid;
4-[(AMinocarbonyl)aMino]-N-[(9H-fluoren-9-ylMethoxy)carbonyl]-D-phenylalanine;
5-Fmoc-D-4-Aph(cBm)-OH



Chemical & Physical Properties
Appearance: White to Off-White Solid
Assay: NLT99%
Melting Point: 163 ℃(decomposition)
Boiling point: 699.1±55.0 ℃(Predicted)
Flash Point: 376.6±31.5 ℃
Density: 1.376±0.06 g/cm3(Predicted)
Solubility: DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
Stability: Hygroscopic



Application: Fmoc-D-4-Aph(cBm)-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize biologically active peptide mimetics, such as Ac-D2Nal-D4Cpa-D3Pal-Ser-4Aph/4Amf(P)-D4Aph/D4Amf(Q)-Leu-ILys-Pro-DAla-NH2 with gonadotropin-releasing hormone (GnRH) antagonist activity.



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