N-Boc-L-valine, 98+%

CAS: 13734-41-3 | C10H19NO4 | 217.27 g/mol

產品號碼	Quantity
A16007.14 亦稱為 A16007-14	25 g

產品號碼 A16007.14

亦稱為 A16007-14

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CAS13734-41-3

IUPAC Name(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-methylbutanoic acid

Molecular FormulaC10H19NO4

InChI KeySZXBQTSZISFIAO-ZETCQYMHSA-N

SMILESCC(C)[C@H](NC(=O)OC(C)(C)C)C(O)=O

Melting Point (clear melt)74.0-81.0?C

Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%

Identification (FTIR)Conforms

Optical Rotation-7.4 ± 0.5? (C=1 in acetic acid)

Appearance (Color)White

N-Boc-L-valine is used in the multi-peptide synthesis and serves as the amino acid protection monomer.

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
N-Boc-L-valine is used in the multi-peptide synthesis and serves as the amino acid protection monomer.

Solubility
Insoluble in water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.

RUO – Research Use Only

General References:

Masami Kuriyama; Takahiro Soeta; Xinyu Hao; Qian Chen; Kiyoshi Tomioka. N-Boc-L-Valine-Connected Amidomonophosphane Rhodium(I) Catalyst for Asymmetric Arylation of N-Tosylarylimines with Arylboroxines. J. Am. Chem. Soc. 2004, 126, (26),8128-8129
Takahiro Soeta; Masami Kuriyama; Kiyoshi Tomioka. Catalytic asymmetric conjugate addition of dialkylzinc reagents to β-aryl-α,β-unsaturated N-2,4,6-triisopropylphenylsulfonylaldimines with use of N-Boc-l-Val-connected amidophosphane-copper(I) catalyst. J. Org. Chem. 2005, 70, (1),297-300