m-Toluoyl Chloride TCI T0309

Chemical Identity

CAS No.: 1711-06-4
PubChem: CID 74375·SID 87576284
Formula: C8H7ClO
Molecular weight: 154.59 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-methylbenzoyl chloride
SMILES: CC1=CC(=CC=C1)C(=O)Cl
InChIKey: YHOYYHYBFSYOSQ-UHFFFAOYSA-N

Rp 1.008.000,00

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m-Toluoyl Chloride (CAS 1711-06-4) is a versatile organic compound widely used in laboratory settings for its reactivity and utility in synthetic chemistry. It serves as a key building block in the synthesis of aromatic and heterocyclic compounds, making it an essential reagent in organic chemistry research. Its ability to participate in electrophilic substitution and coupling reactions makes it a valuable tool for chemists working on complex molecule synthesis. This compound is commonly found in academic and industrial laboratories where organic synthesis is a core activity.

The chemical and physical properties of m-Toluoyl Chloride make it a preferred choice for specific synthetic applications. It is a stable molecular structure but highly sensitive to moisture and air, requiring careful handling. It appears as a white solid and dissolves readily in organic solvents such as ethyl acetate and chloroform. These solubility characteristics make it ideal for reactions that require anhydrous conditions. Its reactivity and solubility profile enable it to be used in a variety of synthetic pathways, enhancing its applicability in laboratory research.

In Indonesian laboratories, m-Toluoyl Chloride is extensively used in organic chemistry research, particularly in educational institutions and research centers. Its role in the synthesis of pharmaceuticals, materials, and specialty chemicals makes it a critical component in both academic and industrial research. It is commonly used in projects involving the development of new compounds and the study of reaction mechanisms. Its availability and reliability make it a trusted reagent in the Indonesian scientific community.

Related TCI products

Organic Synthesis: m-Toluoyl Chloride is widely used in the synthesis of aromatic and heterocyclic compounds due to its reactivity in electrophilic substitution reactions.
Pharmaceutical Research: It plays a key role in the development of new drug compounds, particularly in the synthesis of aromatic derivatives and functionalized molecules.
Material Science: The compound is utilized in the creation of advanced materials, including polymers and specialty chemicals, due to its structural versatility.
Analytical Chemistry: It serves as a reagent in various analytical techniques, aiding in the identification and quantification of organic compounds.
Teaching and Education: It is commonly used in academic laboratories to demonstrate fundamental organic reactions and synthetic methodologies to students.

Brand	TCI
CAS number	1711-06-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	White solid
Storage	Should be stored in a dry, cool, and airtight container away from moisture and light

m-Toluoyl Chloride should be stored in a dry, cool, and airtight container to prevent moisture absorption and degradation. It is sensitive to both humidity and air, so it is essential to use suitable containers such as glass or sealed plastic vessels. In laboratory settings, it should be handled with care, using appropriate personal protective equipment such as gloves and goggles. Due to its reactivity, it is recommended to store it in a well-ventilated area away from incompatible substances. Regular monitoring of storage conditions ensures the compound remains stable and effective for use in chemical reactions. Proper handling and storage protocols are crucial to maintaining its integrity and ensuring safe laboratory practices.

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