CAS 152120-54-2

N,N'-bis-boc-1-guanylpyrazole

Description:

N,N'-bis-Boc-1-guanylpyrazole is a chemical compound characterized by its unique structure, which includes a pyrazole ring and two tert-butyloxycarbonyl (Boc) protecting groups. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The Boc groups serve to protect the amine functionalities during reactions, allowing for selective modifications of the pyrazole moiety. N,N'-bis-Boc-1-guanylpyrazole is known for its potential biological activity, often acting as a precursor in the synthesis of guanidine derivatives, which can exhibit various pharmacological properties. The compound is generally stable under standard laboratory conditions but may require specific handling and storage to maintain its integrity. Its solubility can vary depending on the solvent used, and it is important to consider its reactivity in the context of the desired synthetic pathway. Overall, N,N'-bis-Boc-1-guanylpyrazole is a valuable intermediate in chemical research and development.

Formula: C₁₄H₂₂N₄O₄

InChI: InChI=1/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)

SMILES: CC(C)(C)OC(=O)N=C(N=C(O)OC(C)(C)C)n1cccn1

Synonyms:

• N,N'-bis-(t-butyl-oxycarbonyl)-1-guanylpyrazole
• N,N'-bis-(tert-butyloxycarbonyl)-1-guanylpyrazole
• Pyrazole(Boc)2
• Pyrazol(Boc)2
• N,N'-bis-(tert-butoxycarbonyl)-1-guanylpyrazole
• N,N'-diboc-1h-pyrazole guanidine
• N,N-bis-(t-butyloxycarbonyl)-1-guanylpyrazole, N,N-di-boc-1h-pyrazole-1-carboxamidine
• N,N'-bis-boc-1-guanylpyrazol
• di-tert-butyl (1H-pyrazol-1-ylmethylylidene)biscarbamate
• N,N'-Di-Boc-1H-pyrazole-1-carboxamidine

N,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine

CAS: 152120-54-2

Formula: C₁₄H₂₂N₄O₄

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 310.35

Ref: 3B-B3619

N,N'-Di-Boc-1H-pyrazole-1-carboxamidine, 98+%

CAS: 152120-54-2

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 legac

Formula: C₁₄H₂₂N₄O₄

Purity: 98+%

Molecular weight: 310.35

Ref: 02-H54565

N,N-Bis-Boc-1-Guanylpyrazole

CAS: 152120-54-2

Formula: C₁₄H₂₂N₄O₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 310.3489

Ref: IN-DA0035B1

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

CAS: 152120-54-2

Formula: C₁₄H₂₂N₄O₄

Purity: ≥ 98.0%

Color and Shape: White to almost white powder

Molecular weight: 310.35

Ref: 7W-GM7379

1H-Pyrazole-1-carboxamidine, N,N'-Bis-BOC protected

CAS: 152120-54-2

1H-Pyrazole-1-carboxamidine, N,N'-Bis-BOC protected

Formula: C₁₄H₂₂N₄O₄

Purity: 98%

Color and Shape: white solid

Molecular weight: 310.35g/mol

Ref: 54-OR40453

Bis-Boc-pyrazolocarboxamidine

CAS: 152120-54-2

Formula: C₁₄H₂₂N₄O₄

Purity: 95%

Color and Shape: Solid, Powder or Crystalline Powder

Molecular weight: 310.354

Ref: 10-F047665

N,N'-Bis-Boc-1-guanylpyrazol

CAS: 152120-54-2

N,N'-Bis-Boc-1-guanylpyrazol is a tetrapeptide that is used as a reagent in organic synthesis. It has been shown to have an inhibitory effect on the production and release of melanocortin and its related peptides, which are important for the regulation of body weight, appetite, and mood. N,N'-Bis-Boc-1-guanylpyrazol binds to sulfate groups on chondroitin sulfate proteoglycans. The inhibition of these sulfated proteoglycans leads to decreased levels of hyaluronic acid and a lack of water retention in the joints. This can cause symptoms such as pain and stiffness in joints, particularly those affected by osteoarthritis.

Formula: C₁₄H₂₂N₄O₄

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 310.35 g/mol

Ref: 3D-FB39275

N,N’-Bis-boc-1-guanylpyrazole

Controlled Product

CAS: 152120-54-2

Applications N,N'-Bis-Boc-1-guanylpyrazole is used in the stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin.
References Swift, M., et al.: Org. Biomol. Chem., 4, 3889 (2006), Reid, C., et al.: Bioorg. Med. Chem. Lett., 18, 5399 (2008),

Formula: C₁₄H₂₂N₄O₄

Color and Shape: Neat

Molecular weight: 310.35

Ref: TR-B414125