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Sku CI00799_1_G
Chem Impex
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Product Information

Product Name
4,4',4"-Trimethoxytrityl chloride
Brand Name
Chem Impex
Product Number
00799
CAS
49757-42-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
630505
IUPAC Name
1-chloro-bis(4-methoxyphenyl)methyl-4-methoxybenzene
InChI Key
OBFCMKPFILBCSQ-UHFFFAOYSA-N
SMILES
COC1=CC=C(C=C1)C(C2=CC=C(C=C2)OC)(C3=CC=C(C=C3)OC)Cl

Application

4,4',4"-Trimethoxytrityl chloride is widely utilized in research focused on:

Nucleic Acid Synthesis: This compound serves as a protecting group in the synthesis of oligonucleotides, enhancing the efficiency and yield of DNA and RNA production.

Pharmaceutical Development: It plays a crucial role in the development of new drugs by facilitating the modification of nucleosides and nucleotides, which are vital for therapeutic agents.

Biotechnology: The compound is used in various biotechnological applications, including gene therapy, where it aids in the stabilization of genetic materials.

Analytical Chemistry: It acts as a reagent in analytical methods, improving the detection and quantification of specific biomolecules in complex mixtures.

Research Laboratories: Commonly found in academic and industrial labs, it is essential for researchers working on chemical modifications and synthesis of complex organic molecules.

References

Synthesis and biological evaluation of α- and β-hydroxy substituted amino acid derivatives as potential mGAT1–4 inhibitors

Publication Name: Medicinal Chemistry Research
Publication Date: 2020-05-08
DOI: 10.1007/s00044-020-02548-x

Photoinitiated cationic polymerization of epoxide and vinyl monomers by p-trimethoxytrityl salts

Publication Name: Journal of Polymer Research
Publication Date: 2006-12-14
DOI: 10.1007/s10965-006-9086-2

ET and Polar Mechanisms; How Are They Connected?

Publication Name: Reactivity and Structure Concepts in Organic Chemistry
Publication Date: 1987
DOI: 10.1007/978-3-642-72544-9_11

S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198