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N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

CAS# 152120-54-2

N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

Catalog No. BCC9065----Order now to get a substantial discount!

Product Name & Size Price Stock
N,N'-Di-Boc-1H-pyrazole-1-carboxamidine: 5mg $17 In Stock
N,N'-Di-Boc-1H-pyrazole-1-carboxamidine: 10mg Please Inquire In Stock
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N,N'-Di-Boc-1H-pyrazole-1-carboxamidine: 50mg Please Inquire Please Inquire
N,N'-Di-Boc-1H-pyrazole-1-carboxamidine: 100mg Please Inquire Please Inquire
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N,N'-Di-Boc-1H-pyrazole-1-carboxamidine: 500mg Please Inquire Please Inquire
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Quality Control of N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

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Chemical structure

N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

3D structure

Chemical Properties of N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

Cas No. 152120-54-2 SDF Download SDF
PubChem ID 6383521 Appearance Powder
Formula C14H22N4O4 M.Wt 310.3
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name tert-butyl (NZ)-N-[[(2-methylpropan-2-yl)oxycarbonylamino]-pyrazol-1-ylmethylidene]carbamate
SMILES CC(C)(C)OC(=O)NC(=NC(=O)OC(C)(C)C)N1C=CC=N1
Standard InChIKey QFNFDHNZVTWZED-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H22N4O4/c1-13(2,3)21-11(19)16-10(18-9-7-8-15-18)17-12(20)22-14(4,5)6/h7-9H,1-6H3,(H,16,17,19,20)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

N,N'-Di-Boc-1H-pyrazole-1-carboxamidine Dilution Calculator

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N,N'-Di-Boc-1H-pyrazole-1-carboxamidine Molarity Calculator

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Preparing Stock Solutions of N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.2227 mL 16.1134 mL 32.2269 mL 64.4538 mL 80.5672 mL
5 mM 0.6445 mL 3.2227 mL 6.4454 mL 12.8908 mL 16.1134 mL
10 mM 0.3223 mL 1.6113 mL 3.2227 mL 6.4454 mL 8.0567 mL
50 mM 0.0645 mL 0.3223 mL 0.6445 mL 1.2891 mL 1.6113 mL
100 mM 0.0322 mL 0.1611 mL 0.3223 mL 0.6445 mL 0.8057 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors.[Pubmed:28518069]

J Vis Exp. 2017 Apr 27;(122).

The guanidine group is one of the most important pharmacophoric groups in medicinal chemistry. The only amino acid carrying a guanidine group is arginine. In this article, an easy method for the modification of the guanidine group in peptidic ligands is provided, with an example of RGD-binding integrin ligands. It was recently demonstrated that the distinct modification of the guanidine group in these ligands allows for the selective modulation of the subtype (e.g., between the subtypes alphav and alpha5). Moreover, a formerly unknown strategy for the functionalization via the guanidine group was demonstrated, and the synthetic approach is reviewed in this document. The modifications described here involve terminally (Nomega) alkylated and acetylated guanidine groups. For the synthesis, tailor-made precursor molecules are synthesized, which are then subjected to a reaction with an orthogonally deprotected amine to transfer the pre-modified guanidine group. For the synthesis of alkylated guanidines, precursors based on N,N'-Di-Boc-1H-pyrazole-1-carboxamidine are used to synthesize acylated compounds, the precursor of choice being a correspondingly acylated derivative of N-Boc-S-methylisothiourea, which can be obtained in one- and two-step reactions.

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