Ethyl 4-Bromo-3-methylbenzoate TCI E1036

Chemical Identity

Other names: 4-Bromo-3-methylbenzoic Acid Ethyl Ester · Ethyl 4-Bromo-m-toluate · 4-Bromo-m-toluic Acid Ethyl Ester
CAS No.: 160313-69-9
PubChem: CID 21729626·SID 354333158
Formula: C10H11BrO2
Molecular weight: 243.10 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 4-bromo-3-methylbenzoate
SMILES: CCOC(=O)C1=CC(=C(C=C1)Br)C
InChIKey: GIGDAWLJINYIFV-UHFFFAOYSA-N
MDL: MDL00673007

Rp 795.900,00

Sale Sold out

Shipping calculated at checkout.

Berat 5g 25g

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

Ethyl 4-Bromo-3-methylbenzoate is a chemical compound widely used in organic synthesis reactions, particularly in the formation of aromatic compounds and their derivatives. This reagent plays a crucial role in laboratory settings as a building block for the synthesis of complex molecules with aromatic or heteroaromatic structures. Its versatility makes it a valuable component in various synthetic pathways, especially those involving electrophilic substitution reactions. The compound's ability to act as an electron donor or a substrate in such reactions enhances its utility in synthetic chemistry.

The compound's stable molecular structure and predictable chemical behavior make it a preferred choice for researchers. It exhibits consistent reactivity under controlled conditions, allowing for precise control over synthetic outcomes. This reliability is essential in laboratory environments where reproducibility and accuracy are paramount. Its chemical properties are well-documented, enabling chemists to anticipate reaction pathways and optimize experimental conditions effectively.

In Indonesian laboratories, Ethyl 4-Bromo-3-methylbenzoate is commonly used in research across multiple disciplines, including pharmacology, organic chemistry, and the synthesis of bioactive compounds. Its relevance stems from its ability to participate in bromo substitution reactions on aromatic rings, making it a key reagent for the development of new compounds with specific functional groups. Its application is particularly valuable in the study of aromatic substitution mechanisms and the design of novel synthetic routes.

Related TCI products

Organic Synthesis: Ethyl 4-Bromo-3-methylbenzoate is ideal for creating aromatic compounds with bromo and methyl substitutions, supporting the development of new pharmaceuticals and materials.
Pharmacological Research: The compound is used to synthesize bioactive molecules, aiding in the discovery of new drugs and therapeutic agents.
Heteroaromatic Compound Synthesis: Its reactivity makes it suitable for reactions leading to heteroaromatic structures, which are common in medicinal chemistry.
Electrophilic Substitution Studies: The compound's role as a substrate allows for detailed investigation of substitution mechanisms in aromatic systems.
Teaching and Training: It serves as an educational tool for students and researchers to understand synthetic pathways and reactivity patterns.

Brand	TCI
CAS number	160313-69-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid, crystalline
Storage	Store in a cool, dry place away from light and moisture

Ethyl 4-Bromo-3-methylbenzoate should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. As a chemical reagent, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with skin and eyes, and follow standard laboratory safety protocols to minimize risk. Its chemical nature requires careful handling to maintain its integrity and ensure safe use in experimental procedures.

—