What is the PHENYLTHIOHYDANTOIN-TRYPTOPHAN?

PHENYLTHIOHYDANTOIN-TRYPTOPHAN is , while it's Molecular Formula is C18H15 N3 O S. Used in Biochemistry Research: PHENYLTHIOHYDANTOIN-TRYPTOPHAN is used as a key reagent in the Edman degradation method for protein sequencing. It facilitates the identification and analysis of the N-terminal amino acid in a protein sequence, which is crucial for understanding the structure and function of proteins. Used in Pharmaceutical Research: In the pharmaceutical industry, PHENYLTHIOHYDANTOIN-TRYPTOPHAN is utilized for the development and analysis of protein-based drugs. Its role in protein sequencing aids in the discovery of new therapeutic agents and the optimization of existing ones, contributing to advancements in drug design and development.

What is the CAS number for PHENYLTHIOHYDANTOIN-TRYPTOPHAN?

The CAS number of PHENYLTHIOHYDANTOIN-TRYPTOPHAN is 5789-24-2.

What is PHENYLTHIOHYDANTOIN-TRYPTOPHAN (5789-24-2) used for?

PHENYLTHIOHYDANTOIN-TRYPTOPHAN is a chemical compound derived from the reaction of phenylisothiocyanate with tryptophan, resulting in a phenylthiohydantoin derivative. It is integral to the process of protein sequencing, playing a pivotal role in the Edman degradation method, which is used to determine the sequence of amino acids in proteins.InChI:InChI=1/C18H15N3OS/c22-17-16(10-12-11-19-15-9-5-4-8-14(12)15)20-18(23)21(17)13-6-2-1-3-7-13/h1-9,11,16,19H,10H2,(H,20,23)

What is the PHENYLTHIOHYDANTOIN-TRYPTOPHAN?

PHENYLTHIOHYDANTOIN-TRYPTOPHAN is , while it's Molecular Formula is C18H15 N3 O S. Used in Biochemistry Research: PHENYLTHIOHYDANTOIN-TRYPTOPHAN is used as a key reagent in the Edman degradation method for protein sequencing. It facilitates the identification and analysis of the N-terminal amino acid in a protein sequence, which is crucial for understanding the structure and function of proteins. Used in Pharmaceutical Research: In the pharmaceutical industry, PHENYLTHIOHYDANTOIN-TRYPTOPHAN is utilized for the development and analysis of protein-based drugs. Its role in protein sequencing aids in the discovery of new therapeutic agents and the optimization of existing ones, contributing to advancements in drug design and development.

What is the CAS number for PHENYLTHIOHYDANTOIN-TRYPTOPHAN?

The CAS number of PHENYLTHIOHYDANTOIN-TRYPTOPHAN is 5789-24-2.

What is PHENYLTHIOHYDANTOIN-TRYPTOPHAN (5789-24-2) used for?

PHENYLTHIOHYDANTOIN-TRYPTOPHAN is a chemical compound derived from the reaction of phenylisothiocyanate with tryptophan, resulting in a phenylthiohydantoin derivative. It is integral to the process of protein sequencing, playing a pivotal role in the Edman degradation method, which is used to determine the sequence of amino acids in proteins.InChI:InChI=1/C18H15N3OS/c22-17-16(10-12-11-19-15-9-5-4-8-14(12)15)20-18(23)21(17)13-6-2-1-3-7-13/h1-9,11,16,19H,10H2,(H,20,23)

Manufacturer supply high quality PHENYLTHIOHYDANTOIN-TRYPTOPHAN 5789-24-2 with ISO standards

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PHENYLTHIOHYDANTOIN-TRYPTOPHAN

CAS No.: 5789-24-2
Purity: 99%

Manufacturer supply high quality PHENYLTHIOHYDANTOIN-TRYPTOPHAN 5789-24-2 with ISO standards

Molecular Formula: C18H15 N3 O S
Molecular Weight: 321.403
Vapor Pressure: 7.95E-11mmHg at 25°C
Melting Point: 183 °C
Boiling Point: 538.8°Cat760mmHg
PKA: 11.12±0.40(Predicted)
Flash Point: 236.1°C
PSA： 80.22000
Density: 1.156g/cm³
LogP: 3.39410

PHENYLTHIOHYDANTOIN-TRYPTOPHAN(Cas 5789-24-2) Usage

General Description

Phenylthiohydantoin-tryptophan is a chemical compound used in the process of sequencing proteins. It is formed by the reaction of phenylisothiocyanate with tryptophan, resulting in the formation of a phenylthiohydantoin derivative of tryptophan. PHENYLTHIOHYDANTOIN-TRYPTOPHAN is used in the Edman degradation method, a technique for determining the sequence of amino acids in a protein. It works by cleaving the N-terminal amino acid and converting it into a derivative that can be identified and analyzed. Phenylthiohydantoin-tryptophan plays a crucial role in protein sequencing and has applications in biochemistry and pharmaceutical research.

InChI:InChI=1/C18H15N3OS/c22-17-16(10-12-11-19-15-9-5-4-8-14(12)15)20-18(23)21(17)13-6-2-1-3-7-13/h1-9,11,16,19H,10H2,(H,20,23)