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Thermo Scientific Chemicals
N-Boc-guanidine, 95%
CAS: 219511-71-4 | C6H13N3O2 | 159.189 g/mol
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Catalog number H63206.06
also known as H63206-06
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64.65
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Quantity:
5 g
Price (USD)
64.65
Online Exclusive
71.70Save 7.05 (10%)
Each
Chemical Identifiers
CAS219511-71-4
IUPAC Nametert-butyl N-(diaminomethylidene)carbamate
Molecular FormulaC6H13N3O2
InChI KeyUMOZLQVSOVNSCA-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)N=C(N)N
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale yellow
FormPowder
Assay (unspecified)≥94.0%
N-Boc-guanidine, is used as used as guanidinylating agent and for synthesis of 2-aminoimidazoles. It is also used as a pharmaceutical intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
N-Boc-guanidine, is used as used as guanidinylating agent and for synthesis of 2-aminoimidazoles. It is also used as a pharmaceutical intermediate.
Solubility
Soluble in most alcohols, esters (e.g., ethyl acetate), ketones (e.g., acetone), acetonitrile, and dichloromethane. Not soluble in diethyl ether and hexane.
Notes
Moisture, heat sensitive. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
N-Boc-guanidine, is used as used as guanidinylating agent and for synthesis of 2-aminoimidazoles. It is also used as a pharmaceutical intermediate.
Solubility
Soluble in most alcohols, esters (e.g., ethyl acetate), ketones (e.g., acetone), acetonitrile, and dichloromethane. Not soluble in diethyl ether and hexane.
Notes
Moisture, heat sensitive. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only
General References:
- C Schroif-Grégoire.; K Barale.; A Zaparucha. Preparation of N-alkyl-N'-carboalkoxy guanidines: unexpected effective trans-alkoxylation transforming the 2, 2, 2-trichloroethoxycarbonyl into various carbamates. Tetrahedron letters.200748 (13), 2357-2359.
- CW Zapf.; CJ Creighton.; M Tomioka.; M Goodman. A novel traceless resin-bound guanidinylating reagent for secondary amines to prepare N, N-disubstituted guanidines. Organic letters.20013 (8), 1133-1136.