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N,N'-Di-Boc-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals
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Catalog number H54565.03
also known as H54565-03
Price (USD)/ Each
36.90
-
Quantity:
1 g
Price (USD)/ Each
36.90
N,N'-Di-Boc-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals
Catalog numberH54565.03
Price (USD)/ Each
36.90
-
Chemical Identifiers
CAS152120-54-2
IUPAC Nametert-butyl N-({[(tert-butoxy)carbonyl]imino}(1H-pyrazol-1-yl)methyl)carbamate
Molecular FormulaC14H22N4O4
InChI KeyQFNFDHNZVTWZED-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)NC(=NC(=O)OC(C)(C)C)N1C=CC=N1
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)98.0% min
N,N'-Di-Boc-1H-pyrazole-1-carboxamidine is used in the stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin.
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,N′-Di-Boc-1H-pyrazole-1-carboxamidine is used in the stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin.
Solubility
Slightly soluble in water. Soluble in methanol, and chloroform.
Notes
Store at 4°C.
N,N′-Di-Boc-1H-pyrazole-1-carboxamidine is used in the stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin.
Solubility
Slightly soluble in water. Soluble in methanol, and chloroform.
Notes
Store at 4°C.
RUO – Research Use Only
General References:
- Gregory J. Gabriel.; Ahmad E. Madkour.; Jeffrey M. Dabkowski.; Christopher F. Nelson.; Klaus Nüsslein.; Gregory N. Tew. Synthetic Mimic of Antimicrobial Peptide with Nonmembrane-Disrupting Antibacterial Properties.Biomacromolecules. 2008, 9 (11),2980-2983.
- Luca Gentilucci.; Giuliana Cardillo.; Federico Squassabia.; Alessandra Tolomelli.; Santi Spampinato.; Antonino Sparta.; Monica Baiula. Inhibition of cancer cell adhesion by heterochiral Pro-containing RGD mimetics. Bioorg. Med. Chem. Lett. 2007, 17 (8),2329-2333.