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 | Aaron Chemicals LLC | ₹ 342.24 - ₹ 41,411.04 | |
 | tert-Butyl (4-aminophenyl)carbamate | ChemScene | ₹ 1,026.72 - ₹ 51,250.44 | |
 | 71026-66-9 | 4-(tert-Butoxycarbonylamino)aniline | A2B Chem | ₹ 427.80 - ₹ 7,187.04 |
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
Compare Similar Items
Show Difference
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
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
Quality Level: 100
Assay: ≥99.0% (T)
form: __
reaction suitability: reaction type: Boc solid-phase peptide synthesis
functional group: __
SMILES string: CC(C)(C)OC(=O)N[C@H](C(O)=O)c1ccccc1
InChI: 1S/C13H17NO4/c1-13(2,3)18-12(17)14-10(11(15)16)9-7-5-4-6-8-9/h4-8,10H,1-3H3,(H,14,17)(H,15,16)/t10-/m0/s1
InChI key: HOBFSNNENNQQIU-JTQLQIEISA-N
Quality Level:
100
Assay:
≥99.0% (T)
form:
__
reaction suitability:
reaction type: Boc solid-phase peptide synthesis
functional group:
__
SMILES string:
CC(C)(C)OC(=O)N[C@H](C(O)=O)c1ccccc1
InChI:
1S/C13H17NO4/c1-13(2,3)18-12(17)14-10(11(15)16)9-7-5-4-6-8-9/h4-8,10H,1-3H3,(H,14,17)(H,15,16)/t10-/m0/s1
InChI key:
HOBFSNNENNQQIU-JTQLQIEISA-N
Quality Level: 100
Assay: ≥99.0% (T)
form: solid
reaction suitability: reaction type: Boc solid-phase peptide synthesis
functional group: __
SMILES string: CC(C)(C)OC(=O)N1CCC[C@H]1C(O)=O
InChI: 1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1
InChI key: ZQEBQGAAWMOMAI-ZETCQYMHSA-N
Quality Level:
100
Assay:
≥99.0% (T)
form:
solid
reaction suitability:
reaction type: Boc solid-phase peptide synthesis
functional group:
__
SMILES string:
CC(C)(C)OC(=O)N1CCC[C@H]1C(O)=O
InChI:
1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1
InChI key:
ZQEBQGAAWMOMAI-ZETCQYMHSA-N
Quality Level: 200
Assay: ≥99.9%
form: liquid
reaction suitability: __
functional group: __
SMILES string: __
InChI: __
InChI key: __
Quality Level:
200
Assay:
≥99.9%
form:
liquid
reaction suitability:
__
functional group:
__
SMILES string:
__
InChI:
__
InChI key:
__