692-99-9

Basic information

• Product Name: Carbamic acid, thio-, O-butyl ester
• Synonyms: Carbamic acid, thio-, O-butyl ester
• CAS NO: 692-99-9
• Molecular Formula: C₅H₁₁NOS
• Molecular Weight: 0
• Mol File: 692-99-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbamic acid, thio-, O-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, thio-, O-butyl ester(692-99-9)
• EPA Substance Registry System: Carbamic acid, thio-, O-butyl ester(692-99-9)

Safety Data

• Hazardous Substances Data: 692-99-9(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 71-36-3 butan-1-ol 
• 871-58-9 potassium butylxanthate 
• 1768-24-7 Cyansaeure-n-butylester 
• 802028-88-2 hydrazinecarbothioic acid O-butyl ester 

Downstream Products

• 19968-32-2 5-(4-chloro-phenylsulfanyl)-4-methyl-3H-thiazol-2-one 
• 19968-41-3 4-(4-chloro-phenyl)-5-(4-chloro-phenylsulfanyl)-3H-thiazol-2-one 
• 1313593-22-4 C₁₆H₂₅NO₃S₂ 
• 17425-14-8 O-butyl N-phenylcarbamothioate 
• 1400685-08-6 C₁₆H₂₁NO₂S 
• 1415231-55-8 C₂₀H₂₅NO₃S₂ 
• 1415231-54-7 C₁₄H₂₁NO₃S₂ 
• 19968-39-9 5-(3,4-dichloro-phenylsulfanyl)-4-phenyl-3H-thiazol-2-one 
• 19968-37-7 5-(2,4-dichloro-phenylsulfanyl)-4-phenyl-3H-thiazol-2-one 
• 19968-33-3 5-(2,4-dichloro-phenylsulfanyl)-4-methyl-3H-thiazol-2-one 
• 19968-36-6 5-(4-chloro-phenylsulfanyl)-4-phenyl-3H-thiazol-2-one 
• 19968-35-5 5-(3,4-dichloro-phenylsulfanyl)-4-methyl-3H-thiazol-2-one 

Relevant articles and documents

An Fe3O4@SiO2/Schiff base/Cu(ii) complex as an efficient recyclable magnetic nanocatalyst for selective mono: N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids

An efficient, convenient and novel method for the selective mono N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids in the presence of a recyclable magnetic Cu(ii) nanocatalyst is described. A variety of mono N-arylated O-alkyl thiocarbamates and O-alkyl carbamates were prepared in good to excellent yields with a broad range of aryl coupling partners. The magnetic nanocatalyst can be easily recovered with an external magnetic field and reused at least five times without noticeable leaching or loss of its catalytic activity. This cost-effective and eco-friendly methodology has some other advantages, such as easy preparation of the catalyst, simple workup procedure, and easy purification, which makes this protocol interesting for the users in various fields of pharmacology and biotechnology systems.

Hairpin folding behavior of mixed α/β-peptides in aqueous solution

The invention of new strategies for the design of protein-mimetic oligomers that manifest the folding encoded in natural amino acid sequences is a significant challenge. In contrast to the α-helix, mimicry of protein β-sheets is less understood. We report