1195-16-0 | 2-Acetamido-4-mercaptobutyric acid gamma-thiolactone

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$25.00	$18.00
5g	95%	in stock	$42.00	$30.00
25g	95%	in stock	$106.00	$75.00
100g	95%	in stock	$356.00	$249.00

Description

• Catalog Number: AA24274
• Chemical Name: 2-Acetamido-4-mercaptobutyric acid gamma-thiolactone
• CAS Number: 1195-16-0
• Molecular Formula: C6H9NO2S
• Molecular Weight: 159.2062
• MDL Number: MFCD00005480
• SMILES: CC(=O)NC1CCSC1=O

Computed Properties

• Complexity: 169
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: -0.3

Upstream Synthesis Route

Citiolone is a versatile compound commonly used in chemical synthesis as a key reagent for various transformations. Its unique chemical structure and properties make it an essential component in many reactions, particularly in organic chemistry. Citiolone is widely employed as a building block in the synthesis of complex molecules and pharmaceuticals due to its ability to undergo diverse chemical reactions.One prominent application of Citiolone in chemical synthesis is its role as a precursor in the production of heterocyclic compounds. By undergoing cyclization reactions with appropriate reagents, Citiolone can facilitate the formation of intricate ring structures commonly found in biologically active compounds. This capability makes Citiolone a valuable tool for chemists involved in the synthesis of pharmaceuticals and agrochemicals.Furthermore, Citiolone serves as a versatile intermediate in the functionalization of organic molecules. Its reactive functional groups allow for the attachment of various substituents, enabling chemists to modify the properties of target compounds. This versatility makes Citiolone a valuable building block in the design and synthesis of novel materials and advanced organic molecules with desired functionalities.In summary, Citiolone plays a crucial role in chemical synthesis by serving as a versatile reagent for diverse transformations. Its applications extend to the synthesis of complex molecules, heterocyclic compounds, pharmaceuticals, and functionalized organic materials, making it an indispensable tool for synthetic chemists striving to create innovative chemical entities.

Literature

• [Conjugation of Plasmodium falciparum Pfs25 to Pseudomonas aeruginosa ExoProtein A with different chemical linkers].

  Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases 20110801

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Organelle specific enzyme markers as indicators of methylmercury neurotoxicity and antidotal efficacy in mice.

  Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine 20030601