N,N'-Bis(carbobenzoxy)-1H-pyrazole-1-carboxamidine TCI B3605

Chemical Identity

CAS No.: 152120-55-3
PubChem: CID 6371643·SID 125307472
Formula: C20H18N4O4
Molecular weight: 378.4 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzyl (NZ)-N-[phenylmethoxycarbonylamino(pyrazol-1-yl)methylidene]carbamate
SMILES: C1=CC=C(C=C1)COC(=O)N/C(=N/C(=O)OCC2=CC=CC=C2)/N3C=CC=N3
InChIKey: NRBUVVTTYMTSKM-UHFFFAOYSA-N

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N,N'-Bis(carbobenzoxy)-1H-pyrazole-1-carboxamidine is a synthetic reagent widely used in laboratory settings for its unique chemical properties. This compound plays a crucial role in organic synthesis, particularly in reactions involving the formation of C-X (non-halogen) bonds. Its complex structure enables it to participate in various chemical transformations, making it a valuable tool for researchers. Due to its stability and reactivity, it is frequently employed in the development of new compounds, especially in pharmaceutical and organic chemistry research.

The compound’s ability to act as both a substrate and an activator in specific reactions makes it a preferred choice for applications requiring precision and control. Its reactivity allows it to engage in peptidation, substitution, and coupling reactions, which are essential in the synthesis of complex molecules. The specificity of its interactions ensures that it can be used in targeted chemical processes without unwanted side reactions. This makes it a reliable reagent for laboratories aiming to achieve high-quality results.

In Indonesian laboratories, this reagent is commonly used in scientific research focused on the synthesis of complex organic compounds. It is a key component in the development of new substances with potential applications in medicine and industry. Many research institutions and universities in Indonesia rely on this compound for their synthetic work, contributing to advancements in chemical and pharmaceutical sciences.

TCI brochures (PDF)

Guanidinylation Reagents 2025-11-07 · p. 1
C-N Bond Formation Reactions 2025-08-07 · p. 6

Related TCI products

Organic synthesis applications benefit from this reagent's ability to form C-X bonds, enabling the creation of complex molecular structures.
Pharmaceutical research utilizes it for the development of new drug compounds due to its reactivity and specificity in targeted chemical reactions.
Peptidation reactions are enhanced by its capacity to act as a coupling agent, facilitating the formation of peptide bonds in synthetic processes.
Research in medicinal chemistry often employs this compound to explore its potential in the synthesis of bioactive molecules.
Industrial chemical development uses it as a versatile reagent for the production of specialty chemicals with specific functional groups.

Brand	TCI
CAS number	152120-55-3
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > C-X(Non-Halogen) Bond Formation [Synthetic Reagents]
Pack sizes	Available in various quantities as per standard reagent packaging
Physical form	Solid or powder, depending on the specific product variant
Storage	Store in a cool, dry place away from moisture and direct sunlight

This reagent should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Proper labeling of storage containers is essential for safety and traceability. Due to its reactivity, it should be handled with care, and appropriate personal protective equipment should be worn when working with it. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with its chemical nature. Always follow standard laboratory safety protocols when handling and storing this compound.

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