CAS 4816-80-2

N-[(4-Methylphenyl)sulfonyl]-L-glutamic acid

Description:

N-[(4-Methylphenyl)sulfonyl]-L-glutamic acid, with the CAS number 4816-80-2, is an organic compound characterized by its sulfonamide functional group and amino acid structure. This compound features a glutamic acid backbone, which is an important amino acid involved in various biological processes, including neurotransmission. The presence of the 4-methylphenylsulfonyl group enhances its chemical properties, potentially influencing its solubility, reactivity, and biological activity. Typically, compounds like this may exhibit properties such as being soluble in polar solvents due to the presence of the sulfonyl group, while the aromatic ring can contribute to hydrophobic interactions. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its structural characteristics suggest potential applications in medicinal chemistry, where modifications to amino acids can lead to novel therapeutic agents. As with many sulfonamides, it may also exhibit antibacterial properties, although specific biological activities would require further investigation.

Formula: C₁₂H₁₅NO₆S

InChI: InChI=1S/C12H15NO6S/c1-8-2-4-9(5-3-8)20(18,19)13-10(12(16)17)6-7-11(14)15/h2-5,10,13H,6-7H2,1H3,(H,14,15)(H,16,17)/t10-/m0/s1

InChI key: InChIKey=KKOZKXBAPIYWAT-JTQLQIEISA-N

SMILES: S(N[C@@H](CCC(O)=O)C(O)=O)(=O)(=O)C1=CC=C(C)C=C1

Synonyms:

• (+)-N-Tosyl-<span class="text-smallcaps">L</span>-glutamic acid
• (+)-p-Toluenesulfonylglutamic acid
• (2S)-2-(4-Methylbenzenesulfonamido)pentanedioic acid
• (2S)-2-{[(4-methylphenyl)sulfonyl]amino}pentanedioate
• (S)-2-[[[4-Methylphenyl)sulfonyl]amino]pentanedioic acid
• <span class="text-smallcaps">L</span>-Glutamic acid, N-[(4-methylphenyl)sulfonyl]-
• Glutamic acid, N-(p-tolylsulfonyl)-
• Glutamic acid, N-(p-tolylsulfonyl)-, <span class="text-smallcaps">L</span>-
• N-(p-Toluenesulfonyl)-L-glutamic Acid
• N-Tosyl-(+)-glutamic acid
• N-[(4-Methylphenyl)sulfonyl]-<span class="text-smallcaps">L</span>-glutamic acid
• N-[(4-methylphenyl)sulfonyl]-D-glutamic acid
• N-[(4-methylphenyl)sulfonyl]-L-glutamic acid
• N-[(4-methylphenyl)sulfonyl]glutamic acid
• N-p-Tolylsulfonyl-<span class="text-smallcaps">L</span>-glutamic acid
• NSC 109186
• Tosylglutamic acid
• p-Toluenesulfonyl-<span class="text-smallcaps">L</span>-glutamic acid
• Glutamic acid, N-(p-tolylsulfonyl)-, L-
• L-Glutamic acid, N-[(4-methylphenyl)sulfonyl]-

(S)-2-(4-Methylphenylsulfonamido)pentanedioic acid

CAS: 4816-80-2

Formula: C₁₂H₁₅NO₆S

Purity: 97%

Color and Shape: Solid

Molecular weight: 301.3156

Ref: IN-DA006WYV

(S)-2-(4-Methylphenylsulfonamido)pentanedioic acid

CAS: 4816-80-2

(S)-2-(4-Methylphenylsulfonamido)pentanedioic acid

Purity: 97%

Molecular weight: 301.32g/mol

Ref: 54-OR1068854

N-Tosyl-L-glutamic Acid

Controlled Product

CAS: 4816-80-2

Formula: C₁₂H₁₅NO₆S

Color and Shape: Neat

Molecular weight: 301.32

Ref: TR-T664985

N-Tosyl-L-glutamic acid

CAS: 4816-80-2

N-Tosyl-L-glutamic acid is an ancillary compound that can be used in organic synthesis. It has been shown to react with ethanol extracts and form an acid complex. The reaction system consists of a water molecule and a nitrogen atom, which is bound to the oxygen atom of the N-tosyl group. This results in a hydrogen bond between the water molecule and the N-tosyl group. In addition, this reaction system has been shown to have luminescence properties. The product is acidic and crystallizes in the monomolecular form. It also exhibits fluorescence properties due to its supramolecular nature.

Formula: C₁₂H₁₅NO₆S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 301.32 g/mol

Ref: 3D-FT28349

(S)-2-(4-Methylphenylsulfonamido)pentanedioic acid

CAS: 4816-80-2

Formula: C₁₂H₁₅NO₆S

Purity: 97%

Molecular weight: 301.31

Ref: 10-F239557