15402

Boc-Dap-OH

≥98.0% (TLC)

• 동의어(들): (S)-2-[(tert-Butoxycarbonyl)amino]-3-aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonyl)aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonylamino)propanoic acid, 3-Amino-(tert-butoxycarbonyl)-L-alanine, Nα-BOC-(S)-β-aminoalanine, Nα-Boc-L-β-aminoalanine, N2-(tert-Butoxycarbonyl)-(S)-2,3-diaminopropionic acid, N2-tert-Butoxycarbonyl-L-2,3-diaminopropionic acid, N_α-Boc-L-2,3-diaminopropionic acid, Boc-Dpr-OH
• 실험식(Hill 표기법): C₈H₁₆N₂O₄
• CAS Number: 73259-81-1
• Molecular Weight: 204.22
• Beilstein: 4182136
• MDL number: MFCD00236843
• UNSPSC 코드: 12352209
• eCl@ss: 32160406
• PubChem Substance ID: 57647411
• NACRES: NA.22

속성

• Quality Level: 100
• 분석: ≥98.0% (TLC)
• 형태: solid
• 광학 활성: [α]20/D +5.5±1°, c = 1% in methanol: water (1:1)
• 반응 적합성: reaction type: Boc solid-phase peptide synthesis
• 불순물: ~3% water
• mp: 210 °C (dec.)
• 응용 분야: peptide synthesis
• SMILES string: CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O
• InChI: 1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
• InChI key: KRJLRVZLNABMAT-YFKPBYRVSA-N

설명

애플리케이션

Reactant for:

• Protein assembly directed by synthetic molecular recognition motifs
• Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities
• Synthesis of HCV protease inhibitor modified analogs
• Solid phase synthesis of peptidic V1a receptor agonists
• Directed peptide assembly at lipid-water interface

기타 정보

Monoprotected derivative of DAP; used e.g. in the synthesis of glucosamine synthase inhibitors, a myosin kinase inhibitor. Preparation of peptides with metal complexing groups.

안전성 정보

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable
• 개인 보호 장비: Eyeshields, Gloves, type N95 (US)