O-Benzyl-L-histidine bis(toluene-p-sulphonate)

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1.What is the O-Benzyl-L-histidine bis(toluene-p-sulphonate) ?

Used in Peptide Synthesis:
O-Benzyl-L-histidine bis(toluene-p-sulphonate) is utilized as a building block in the synthesis of complex proteins and peptides. Its special reactivity and solubility properties facilitate various chemical reactions, contributing to the creation of intricate biomolecular structures.
Used in Biochemistry Research:
In the field of biochemistry, O-Benzyl-L-histidine bis(toluene-p-sulphonate) serves as a valuable tool for studying the interactions and mechanisms of proteins and peptides. The presence of the benzyl group and sulphonate moieties can influence the behavior of these biomolecules, providing insights into their functions and potential applications.

2.What is the CAS number for O-Benzyl-L-histidine bis(toluene-p-sulphonate) ?

The CAS number of O-Benzyl-L-histidine bis(toluene-p-sulphonate) is 24593-59-7.

More information of O-Benzyl-L-histidine bis(toluene-p-sulphonate) 24593-59-7 are:

3.What are another words for O-Benzyl-L-histidine bis(toluene-p-sulphonate) ?

Synonyms?for?O-Benzyl-L-histidine bis(toluene-p-sulphonate) 24593-59-7:O-benzyl-L-histidine bis(toluene-p-sulphonate);L-Histidine benzyl ester di(p-toluenesulfonate) salt;(S)-Benzyl 2-aMino-3-(1H-iMidazol-4-yl)propanoate bis(4-Methylbenzenesulfonate)

4.What is the molecular formula of O-Benzyl-L-histidine bis(toluene-p-sulphonate)?

The chemical formula of ?O-Benzyl-L-histidine bis(toluene-p-sulphonate) is?C27H31N3O8S2 which containing 27 Carbon atoms,31 Hydrogen atoms,3 Nitrogen atoms,8 Oxygen atoms and 2 Sulfur atoms,and the molecular weight of??O-Benzyl-L-histidine bis(toluene-p-sulphonate)?is 589.69.

5.What is O-Benzyl-L-histidine bis(toluene-p-sulphonate) (24593-59-7) used for?

O-Benzyl-L-histidine bis(toluene-p-sulphonate) is a complex organic chemical compound that features the amino acid L-histidine with a benzyl group attached. O-Benzyl-L-histidine bis(toluene-p-sulphonate) also incorporates two toluene-p-sulphonate moieties, a type of sulphonic acid. The combination of these elements endows the compound with unique reactivity and solubility properties, making it valuable in the realm of peptide synthesis and biochemistry.

InChI:InChI=1/C13H15N3O2.2C7H8O3S/c14-12(6-11-7-15-9-16-11)13(17)18-8-10-4-2-1-3-5-10;2*1-6-2-4-7(5-3-6)11(8,9)10/h1-5,7,9,12H,6,8,14H2,(H,15,16);2*2-5H,1H3,(H,8,9,10)/t12-;;/m0../s1

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