Name: BOC-SER-OH >=99.0% T (C005B-032789)
SKU: C005B-032789
Availability: OutOfStock

BOC-SER-OH >=99.0% T (C005B-032789)

Catalog No.

C005B-032789

Manufacturer No.

15500-5G

Manufacturer Name

Sigma-Aldrich

Quantity

Unit of Measure

Boc-Ser-OH is an amino acid derivative. Application Boc-Ser-OH may be used in the synthesis of the following: 2-( N - Fmoc )-3-( N - Boc - N -methoxy)-diaminopropanoic acid (Fmoc: 9-fluorenylmethoxycarbonyl Boc: t-butyloxycarbonyl) Boc-Ser-Leu-OMe

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Description
Specifications

General description

Boc-Ser-OH is an amino acid derivative.

Application

Boc-Ser-OH may be used in the synthesis of the following:

2-(N-Fmoc)-3-(N-Boc-N-methoxy)-diaminopropanoic acid (Fmoc: 9-fluorenylmethoxycarbonyl; Boc: t-butyloxycarbonyl)
Boc-Ser-Leu-OMe
cyclic peptide synthesis
benzylsulfonyl-D-Ser-Ser-4-amidinobenzylamide

Building block in peptide synthesis. Starting material for the synthesis of various α-amino acids via the β-lactone.

Molecular Weight: 205.21. Empirical Formula: C₈H₁₅NO₅. linearFormula: HOCH₂CH(COOH)NHCOOC(CH₃)₃. Quality Level: 100. Assay: ≥. 99.0% (T). optical activity: [α. ]20/D −. 3.5Â±0.5Â°, c : . 2% in acetic acid. reaction suitability: reaction type: Boc solid-phase peptide synthesis. mp: 91 . Â°C (dec.) (lit.). application(s): peptide synthesis. storage temp.: 2-8Â°C. SMILES string: CC(C)(C)OC(: O)N[C@@H](CO)C(O): O. InChI: 1S/C8H15NO5/c1-8(2,3)14-7(13)9-5(4-10)6(11)12/h5,10H,4H2,1-3H3,(H,9,13)(H,11,12)/t5-/m0/s1. InChI key: FHOAKXBXYSJBGX-YFKPBYRVSA-N. Storage Class Code: 11 - Combustible Solids. WGK: WGK 3. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).