531480

Fmoc-Ala-OH

95%, for peptide synthesis

• 동의어(들): N-(9-Fluorenylmethoxycarbonyl)-L-alanine, Fmoc-L-alanine
• 실험식(Hill 표기법): C₁₈H₁₇NO₄
• CAS Number: 35661-39-3
• Molecular Weight: 311.33
• Beilstein: 2225975
• EC Number: 252-660-6
• MDL number: MFCD00037139
• UNSPSC 코드: 12352209
• PubChem Substance ID: 24877820
• NACRES: NA.26

속성

• 제품명: Fmoc-Ala-OH, 95%
• 분석: 95%
• 광학 활성: [α]20/D −18°, c = 1 in DMF
• 반응 적합성: reaction type: C-H Activation; reaction type: Fmoc solid-phase peptide synthesis; reagent type: ligand; reaction type: Peptide Synthesis
• mp: 147-153 °C (lit.)
• 응용 분야: peptide synthesis
• 작용기: Fmoc; amine; carboxylic acid
• 저장 온도: 2-8°C
• SMILES string: C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
• InChI: 1S/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)/t11-/m0/s1
• InChI key: QWXZOFZKSQXPDC-NSHDSACASA-N

설명

일반 설명

Fmoc-Ala-OH also known as Fmoc-L-alanine, is a versatile reagent used in Fmoc solid-phase peptide synthesis.

애플리케이션

Fmoc-Ala-OH is commonly used :

• as a building block in the preparation of triazolopeptides , and azapeptides
• in the synthesis of bis-cationic porphyrin peptides using the standard Fmoc solid-phase synthesis
• to transform Mannich-adducts into α-halogenated amides without undergoing aziridination

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)