15485
N-Boc-p-phenylenediamine
≥97.0% (NT)
Manufacturer: Sigma Aldrich
CAS Number: 71026-66-9
Synonym(S): 4-(tert-Butoxycarbonylamino)aniline, tert-Butyl-4-aminophenylcarbamate
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 25 G | 15485-25-G | In Stock | ₹ 15,100.88 |
15485 - 25 G
In Stock
Quantity
1
Base Price: ₹ 15,100.88
GST (18%): ₹ 2,718.158
Total Price: ₹ 17,819.038
Quality Level
200
Assay
≥97.0% (NT)
form
powder
reaction suitability
reagent type: cross-linking reagent
functional group
Bocamine
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
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
tert-Butyl (4-aminophenyl)carbamate | -- | ₹ 356.00 - ₹ 43,076.00 | ||
tert-Butyl (4-aminophenyl)carbamate | -- | ₹ 1,068.00 - ₹ 53,311.00 | ||
71026-66-9 | 4-(tert-Butoxycarbonylamino)aniline | -- | ₹ 445.00 - ₹ 7,476.00 |
Related Products
Description
- Application: N-Boc-p-phenylenediamine can be used as:A reactant to prepare perylene monoimide-based dyes for dye-sensitized solar cell applications.[1]A starting material to synthesize covalent organic frameworks, which are used as proton exchange membranes for hydrogen fuel cell applications.[2]A reactant in the synthesis of bestatin derived hydroxamic acids as potent pan-HDAC inhibitors.[3]
- Other Notes: Mono-N-acylated diamine, precursor of different Para-substituted anilines (e.g., 4-azido aniline);[4] Synthesis of photoactivable derivative of ouabaine.[5]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves