CBZ-thiophenyl-L-cysteine
Nanjing Finechem Holdings Co., LTD
Specifications
N/A
Packing & Storage
Packing
Storage Powder -20°C 3 years 4°C 2 years;In solvent -80°C 6 months, -20°C 1 month
Shipping Room temperature in continental US; may vary elsewhere
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General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names CBZ-S-Phenyl-L-Cysteine
Structure
CAS No. 159453-24-4 Boiling Point (℃) 547.5±50.0 °C at 760 mmHg
Molecular Weight 331.386 Melting Point (℃) 94-97 °C(lit.)
Density 1.3±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C17H17NO4S Flash Point (℃) 284.9±30.1 °C
Solubility N/A Autoignition Temperature (℃) N/A
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+:Very toxic
Safety Phrases S1-S28-S45
RIDADR NONH for all modes of transport
WGK Germany  3
SYMPTOMS PREVENTION FIRST AID
Inhalation Cough. Sore throat. Use local exhaust or breathing protection. Fresh air, rest.
Skin Redness. Burning sensation. Itching. Protective gloves. Remove contaminated clothes. Rinse and then wash skin with water and soap.
Eyes Redness. Pain. Wear safety goggles. First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Ingestion Abdominal pain. Nausea. Vomiting. Do not eat, drink, or smoke during work. Wash hands before eating. Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention.
Description N-Carbobenzoxy-S-phenyl-L-cysteine is a cysteine derivative[1].
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-807.
Synonyms
(2R)-2-[(Phenylmethoxy)carbonylamino]-3-(phenylthio)propanoic acid
MFCD00671699
Cbz-S-Phenyl-Cys-OH
CBZ-S-PHENYL-L-CYS-OH
N-Z-S-phenyl-L-cysteine
CBZ-S-Phenyl-L-cyste
RS1YVQMVO1R &&L or R Form
(R)-2-{[(Benzyloxy)carbonyl]amino}-3-(phenylthio)propionic acid
EINECS 441-530-6
N-Cbz-S-phenyl-L-cysteine
L-cysteine,S-Phen
N-Carbobenzoxy-S-phenyl-L-cysteine
N-[(Benzyloxy)carbonyl]-S-phenylcysteine
N-CBZ-PHENYL-L-CYSTEINE
Product Description
CBZ-Thiophenyl-L-Cysteine is a cutting-edge chemical compound specifically designed to provide exceptional protection for amino acids during various chemical processes. With its remarkable properties and versatile applications in the field of chemical synthesis, CBZ-Thiophenyl-L-Cysteine has gained significant recognition in the global market. This product introduction aims to highlight the key features, benefits, and potential applications of CBZ-Thiophenyl-L-Cysteine, emphasizing its crucial role in safeguarding amino acids and enabling efficient synthesis in the ever-evolving chemical industry.

Advancements in Chemical Engineering: CBZ-Thiophenyl-L-Cysteine represents a significant advancement in chemical engineering, characterized by exceptional stability and compatibility with diverse reaction conditions. Developed through extensive research and state-of-the-art manufacturing techniques, this compound offers superior protection for amino acids, ensuring their integrity and preventing undesired reactions during synthetic procedures.

Unparalleled Amino Acid Protection: CBZ-Thiophenyl-L-Cysteine provides unparalleled protection for amino acids by forming a robust and reversible bond. This protective group effectively shields the amino acid moiety from unwanted interactions, preserving the reactivity of functional groups. The precise control over chemical transformations enhances overall synthetic efficiency, facilitating the production of high-quality amino acid derivatives with excellent yield and purity. CBZ-Thiophenyl-L-Cysteine streamlines downstream processing and reduces production costs.

Broad Applications in Chemical Synthesis: CBZ-Thiophenyl-L-Cysteine finds extensive utility in various chemical synthesis applications due to its exceptional protective properties. It is widely used in peptide synthesis, pharmaceutical manufacturing, and the preparation of complex organic molecules. CBZ-Thiophenyl-L-Cysteine exhibits compatibility with a wide range of solvents and reagents, making it an ideal choice for both traditional and advanced synthetic methodologies.

Global Market Impact: In the highly competitive global chemical market, CBZ-Thiophenyl-L-Cysteine has emerged as a leading solution. Its consistent quality, reliability, and cost-effectiveness have earned it a strong reputation among researchers, scientists, and industry professionals. The product has witnessed a significant surge in demand, attracting a growing customer base across different regions. CBZ-Thiophenyl-L-Cysteine has become an essential tool for chemical manufacturers seeking to optimize their synthetic processes and deliver high-quality amino acid derivatives.

Conclusion: CBZ-Thiophenyl-L-Cysteine revolutionizes amino acid protection in chemical synthesis, offering exceptional stability, compatibility, and reliability. Its broad applications and positive impact on the global market position it as a key component of modern chemical engineering. By choosing CBZ-Thiophenyl-L-Cysteine, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, specialty chemicals, and other complex organic compounds.

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