15485

N-Boc-p-phenylenediamine

≥97.0% (NT)

• Sinónimos: 4-(tert-Butoxycarbonylamino)aniline, tert-Butyl-4-aminophenylcarbamate
• Fórmula lineal: (CH₃)₃COCONHC₆H₄NH₂
• Número de CAS: 71026-66-9
• Peso molecular: 208.26
• Beilstein/REAXYS Number: 2969618
• EC Number: 275-132-7
• MDL number: MFCD00043022
• UNSPSC Code: 12352116
• PubChem Substance ID: 57647460
• NACRES: NA.22

Propiedades

• Quality Level: 200
• assay: ≥97.0% (NT)
• form: powder
• reaction suitability: reagent type: cross-linking reagent
• functional group: Boc; amine
• SMILES string: NC1=CC=C(NC(OC(C)(C)C)=O)C=C1
• InChI: 1S/C11H16N2O2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,12H2,1-3H3,(H,13,14)
• Inchi Key: WIVYTYZCVWHWSH-UHFFFAOYSA-N

Descripción

Application

N-Boc-p-phenylenediamine can be used as:

• A reactant to prepare perylene monoimide-based dyes for dye-sensitized solar cell applications.
• A starting material to synthesize covalent organic frameworks, which are used as proton exchange membranes for hydrogen fuel cell applications.
• A reactant in the synthesis of bestatin derived hydroxamic acids as potent pan-HDAC inhibitors.

Other Notes

Mono-N-acylated diamine, precursor of different Para-substituted anilines (e.g., 4-azido aniline); Synthesis of photoactivable derivative of ouabaine.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302,H317
• pcodes: P261 - P264 - P272 - P280 - P301 + P312 - P302 + P352
• Hazard Classifications: Acute Tox. 4 Oral - Skin Sens. 1
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves