3-Amino-N-methylbenzamide TCI A1067

Chemical Identity

CAS No.: 25900-61-2
PubChem: CID 676526·SID 87562557
Formula: C8H10N2O
Molecular weight: 150.18 g/mol
Purity: >98.0%(HPLC)(qN
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-amino-N-methylbenzamide
SMILES: CNC(=O)C1=CC(=CC=C1)N
InChIKey: PYDQTASEULDNRL-UHFFFAOYSA-N

Rp 2.227.050,00

~~Rp 1.572.900,00~~ Rp 2.227.050,00

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Berat 5g 25g

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3-Amino-N-methylbenzamide is a chemical compound widely used as a foundational building block in the synthesis of complex molecules. Its simple molecular structure plays a crucial role in the formation of both heterocyclic and non-heterocyclic compounds. In laboratory settings, it serves as a key reagent for chemical reactions that require the combination of amino and methyl groups on an aromatic framework. This compound is essential for various synthetic pathways in organic chemistry.

The stability and controlled reactivity of 3-Amino-N-methylbenzamide make it a preferred choice for a range of chemical reactions, including substitution and condensation processes. Its ability to interact with a variety of reagents enhances its versatility in organic synthesis. This characteristic allows chemists to explore multiple synthetic routes and develop new compounds with desired properties. Its reliability and consistent performance in laboratory experiments further solidify its importance in chemical research.

In Indonesian laboratories, 3-Amino-N-methylbenzamide is commonly used in organic chemistry research, both for educational purposes and scientific investigations. Its availability and competitive pricing make it a practical choice for various laboratory needs. The compound is particularly valuable for students and researchers working on synthetic projects, providing a reliable and effective starting material for their experiments.

Related TCI products

Synthesis of heterocyclic compounds for drug development due to its ability to form stable aromatic structures.
Aromatic substitution reactions where the amino and methyl groups provide functional groups for further modification.
Organic condensation reactions as a versatile intermediate for creating complex molecular frameworks.
Educational experiments in undergraduate chemistry courses to teach fundamental synthetic techniques.
Research in pharmaceutical chemistry for the development of new therapeutic agents through molecular design.

Brand	TCI
CAS number	25900-61-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply options
Physical form	Solid
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption, which could affect its stability. Proper ventilation is essential when handling the material to ensure safe working conditions. Avoid exposure to strong oxidizing agents or reactive substances to prevent unwanted chemical interactions. Keep the material away from heat sources and direct sunlight to prevent degradation. Regular inspection of storage conditions ensures the compound remains suitable for use in laboratory applications.

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