Skip to product information
1 of 1

TCI

CAS 114772-38-2

Methyl 2-[4-(Bromomethyl)phenyl]benzoate TCI M1806

Methyl 2-[4-(Bromomethyl)phenyl]benzoate TCI M1806

Chemical Identity

CAS No.
114772-38-2
PubChem
CID 11012181·SID 87558978
Formula
C15H13BrO2
Molecular weight
305.17 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 2-[4-(bromomethyl)phenyl]benzoate
SMILES
COC(=O)C1=CC=CC=C1C2=CC=C(C=C2)CBr
InChIKey
RMXGTMRDXKUUDJ-UHFFFAOYSA-N
Regular price Rp 795.900,00
Regular price Sale price Rp 795.900,00
Sale Sold out
Shipping calculated at checkout.
Berat
Quantity
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

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

Methyl 2-[4-(Bromomethyl)phenyl]benzoate is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules. This compound serves as a building block in various chemical processes, offering versatility in functional group transformations. Its molecular structure enables substitution reactions and cross-coupling mechanisms, making it a valuable tool in synthetic chemistry. Due to its reactivity and structural adaptability, it is frequently utilized in both academic and industrial research settings.

The compound is preferred for its chemical stability under controlled conditions and its ability to participate in a wide range of synthetic pathways. Its bromomethyl group provides a reactive site for further modification, which is essential in the development of pharmaceuticals and specialty chemicals. Additionally, its compatibility with various reaction conditions makes it a reliable choice for chemists working on complex synthesis routes. The compound's molecular design also supports its use in the creation of heterocyclic and non-heterocyclic compounds.

In Indonesian laboratories, this compound is commonly used in pure chemical research, drug development, and organic synthesis. Its specific structure and reactivity make it a key component in the work of researchers and scientists across various institutions. The availability of this compound in different packaging formats ensures its usability in both small-scale and large-scale experiments, supporting a wide range of research needs.

  • Organic synthesis of complex pharmaceutical compounds due to its reactive bromomethyl group and structural versatility.
  • Development of new drugs and chemical intermediates through substitution and cross-coupling reactions.
  • Research in non-heterocyclic building blocks for the creation of diverse chemical structures.
  • Support for academic studies in synthetic chemistry and chemical engineering.
  • Use in industrial chemical processes requiring high reactivity and functional group modification.

Brand TCI
CAS number 114772-38-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes to suit different experimental scales
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of moisture. It is recommended to use airtight containers to prevent exposure to humidity, which can affect its stability. Due to its sensitivity to UV light, it is best kept in a dark storage cabinet or under a light-blocking cover. Proper ventilation should be maintained in the laboratory to ensure safe handling. Always wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Regular monitoring of storage conditions is advised to maintain the compound's integrity and effectiveness in chemical reactions.

—