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  7. (S)-2-(Boc-amino)-3-(Fmoc-amino)propionic acid, 98%

(S)-2-(Boc-amino)-3-(Fmoc-amino)propionic acid, 98%

Product Code. 15469475
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Product Code. 15469475 Supplier Thermo Scientific Alfa Aesar Supplier No. H51964.06
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Fecha estimada de envoi: 07-12-2026
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Description

CAS: 122235-70-5 | C23H26N2O6 | 426.469 g/mol

It has been used in the synthesis of target chelator, the tris-catechol compound 2.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It has been used in the synthesis of target chelator, the tris-catechol compound 2.

Solubility
Soluble in 2ml dimethyl formamide 0.3gram.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 122235-70-5
Molecular Formula C23H26N2O6
Molecular Weight (g/mol) 426.469
MDL Number MFCD00235897
InChI Key MVWPBNQGEGBGRF-IBGZPJMESA-N
Synonym boc-dap fmoc-oh, s-3-9h-fluoren-9-yl methoxy carbonyl amino-2-tert-butoxycarbonyl amino propanoic acid, s-2-boc-amino-3-fmoc-amino propionic acid, 2s-2-tert-butoxycarbonyl amino-3-9h-fluoren-9-ylmethoxy carbonyl amino propanoic acid, l-alanine, n-1,1-dimethylethoxy carbonyl-3-9h-fluoren-9-ylmethoxy carbonyl amino, n-boc-n'-fmoc-l-2,3-diaminopropionic acid, boc-dap fmoc-oh 1g, boc-l-2,3-diaminopropionic acid fmoc, boc-dap fmoc-oh hplc, n-a-boc-n-b-fmoc-l-2,3-diamiopropionic acid
PubChem CID 7019527
IUPAC Name (2S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
SMILES CC(C)(C)OC(=O)NC(CNC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)C(=O)O

Spezifikation

Quantity 5 g
Beilstein 4771385
Solubility Information Soluble in 2ml dimethyl formamide 0.3gram.
Formula Weight 426.47
Percent Purity 98%
Chemical Name or Material (S)-2-(Boc-amino)-3-(Fmoc-amino)propionic acid

RUO – Research Use Only

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