L-Glutamic acid diallyl ester tosylate
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L-Glutamic acid diallyl ester tosylate

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Category
Amino Acids for Stapled Peptide
Catalog number
BAT-007700
CAS number
20845-16-3
Molecular Formula
C11H17NO4·C7H8O3S
Molecular Weight
399.46
L-Glutamic acid diallyl ester tosylate
IUPAC Name
bis(prop-2-enyl) (2S)-2-aminopentanedioate;4-methylbenzenesulfonic acid
Synonyms
Glu(OAll)-OAll TosOH; H-Glu(oall)-oall p-tosylate; H-Glu(OAll)-OAll TosOH; L-Glutamic acid, 1,5-di-2-propen-1-yl ester, 4-methylbenzenesulfonate (1:1); diallyl L-glutamate p-toluene sulfonate; H-Glu(OAll)-OAll inverted exclamation mark currency HCl; (S)-diallyl 2-aminopentanedioate 4-methylbenzenesulfonate; 1,5-bis(prop-2-en-1-yl) (2S)-2-aminopentanedioate; 4-methylbenzene-1-sulfonic acid; bis(prop-2-enyl) (2S)-2-aminopentanedioate; 4-methylbenzenesulfonic acid
Related CAS
1128075-52-4 (hydrochloride)
Appearance
White powder
Purity
≥ 98% (HPLC)
Melting Point
89-95 °C
Boiling Point
556.9 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C11H17NO4.ClH/c1-3-7-15-10(13)6-5-9(12)11(14)16-8-4-2;/h3-4,9H,1-2,5-8,12H2;1H/t9-;/m0./s1
InChI Key
KJPKKZRNVXKKBV-FVGYRXGTSA-N
Canonical SMILES
C=CCOC(=O)CCC(C(=O)OCC=C)N.Cl

L-Glutamic acid diallyl ester tosylate, a versatile chemical compound with diverse applications in chemical synthesis and materials science, finds its utility in various innovative ways.

Polymer Synthesis: Serving as a monomer or comonomer in specialty polymer synthesis, L-Glutamic acid diallyl ester tosylate exhibits its prowess by participating in polymerization reactions. The compound’s reactive ester and allyl groups combine to generate polymers boasting unique mechanical and chemical properties. These distinctive polymers play essential roles in coatings, adhesives, and advanced composite materials, showcasing a blend of creativity and functionality in material design.

Pharmaceutical Intermediates: Within the pharmaceutical realm, L-Glutamic acid diallyl ester tosylate assumes a critical role as an intermediate in the synthesis of diverse drugs and bioactive compounds. Its functional groups facilitate selective chemical modifications, enabling the creation of novel therapeutic agents. This crucial function aids in tailoring molecules for drug discovery and development, highlighting the compound’s contribution to the continuous evolution of pharmaceutical science with a mix of ingenuity and precision.

Surface Modification: Delving into surface modification processes, L-Glutamic acid diallyl ester tosylate showcases its potential to enhance material properties by grafting onto surfaces. This transformative action introduces new functional groups that can enhance hydrophilicity, adhesion, or biocompatibility, elevating surface properties for critical biomedical applications like implants and sensors. The compound’s adaptability in altering surface properties underscores its role in advancing material science with a blend of sophistication and practicality.

Nanomaterials Engineering: Playing a pivotal role in nanomaterials engineering, L-Glutamic acid diallyl ester tosylate functions as a versatile linking or capping agent for nanoparticles. Its ability to stabilize nanoparticles and facilitate further functionalization with chemical groups or biomolecules expands the horizons of nanomaterial applications in domains such as drug delivery, imaging, and catalysis. This adaptability in nanomaterial functionalization underscores its importance in driving innovation at the nanoscale with a fusion of versatility and creativity.

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