15408

N-Boc-1,3-propanediamine

≥97.0% (GC/NT)

• 別名: N-Boc-1,3-diaminopropane, tert-Butyl N-(3-aminopropyl)carbamate
• 化学式: (CH₃)₃COCONH(CH₂)₃NH₂
• CAS番号: 75178-96-0
• 分子量: 174.24
• Beilstein: 3588328
• MDL番号: MFCD00210021
• UNSPSCコード: 12352116
• PubChem Substance ID: 57647415
• NACRES: NA.22

特性

• 品質水準: 100
• アッセイ: ≥97.0% (GC/NT)
• 反応適合性: reagent type: cross-linking reagent
• 屈折率: n20/D 1.454 (lit.); n20/D 1.459
• bp: 203 °C (lit.)
• mp: 22 °C (lit.)
• 密度: 0.998 g/mL at 20 °C (lit.)
• 官能基: Boc; amine
• SMILES記法: NCCCNC(OC(C)(C)C)=O
• InChI: 1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)
• InChI Key: POHWAQLZBIMPRN-UHFFFAOYSA-N

詳細

アプリケーション

• Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–carbohydrate conjugates′: This study discusses the synthesis of derivatives using N-Boc-1,3-propanediamine to develop new antibacterial agents targeting resistant bacterial strains (Yarlagadda et al., 2015).
• Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022).
• Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018).

その他情報

スペルミジン類縁体の合成。薬理学的に活性な化合物の調製。

安全性情報

• ピクトグラム: GHS05,GHS07
• シグナルワード: Danger
• 危険有害性情報: H302,H314
• 注意書き: P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
• 危険有害性の分類: Acute Tox. 4 Oral - Skin Corr. 1B
• 保管分類コード: 8A - Combustible corrosive hazardous materials
• WGK: WGK 3
• 引火点(°F): 228.2 °F - closed cup
• 引火点(℃): 109 °C - closed cup
• 個人用保護具 (PPE): Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter