N,N'-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals
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N,N'-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N,N'-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals

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Catalog number H54092.03
also known as H54092-03
Price (USD)/ Each
88.20
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Quantity:
1 g
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Price (USD)/ Each
88.20
Add to cart
N,N'-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine, 98+%, Thermo Scientific Chemicals
Catalog numberH54092.03
Price (USD)/ Each
88.20
-
Add to cart
Chemical Identifiers
CAS152120-55-3
IUPAC Namebenzyl N-({[(benzyloxy)carbonyl]imino}(1H-pyrazol-1-yl)methyl)carbamate
Molecular FormulaC20H18N4O4
InChI KeyNRBUVVTTYMTSKM-UHFFFAOYSA-N
SMILESO=C(NC(=NC(=O)OCC1=CC=CC=C1)N1C=CC=N1)OCC1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)>98.0%
N,N'-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine is used as 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,N′-Bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine is used as pharmaceutical intermediate.

Notes
Store in a cool, dry place, in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Jonathan B. Baell; Peter J. Duggan; Stewart A. Forsyth; Richard J. Lewise, Y. Phei Lok; Christina I. Schroeder; Nicholas E. Shepherd. Synthesis and biological evaluation of anthranilamide-based non-peptide mimetics of ω-conotoxin GVIA. Tetrahedron. 2006, 62 (31), 7284-7292.
  2. Masood Hosseini; Longguang Jiang; Hans Peter Sørensen; Jan K. Jensen; Anni Christensen; Sarah Fogh; Cai Yuan; Lisbeth M. Andersen; Mingdong Huang; Peter A. Andreasen and Knud J. Jensen. Elucidation of the Contribution of Active Site and Exosite Interactions to Affinity and Specificity of Peptidylic Serine Protease Inhibitors Using Non-Natural Arginine Analogs. Molecular Pharmacology. 2009, 80 (4), 585-597.