21451-32-1

Basic information

• Product Name: 4-(CYCLOHEXYLAMINO)-4-OXOBUTANOIC ACID
• Synonyms: N-CYCLOHEXYL-SUCCINAMIC ACID;TIMTEC-BB SBB000385;4-(CYCLOHEXYLAMINO)-4-OXOBUTANOIC ACID;ASISCHEM C15582
• CAS NO: 21451-32-1
• Molecular Formula: C₁₀H₁₇NO₃
• Molecular Weight: 199.25
• Mol File: 21451-32-1.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(CYCLOHEXYLAMINO)-4-OXOBUTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(CYCLOHEXYLAMINO)-4-OXOBUTANOIC ACID(21451-32-1)
• EPA Substance Registry System: 4-(CYCLOHEXYLAMINO)-4-OXOBUTANOIC ACID(21451-32-1)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 21451-32-1(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 108-91-8 cyclohexylamine 

Downstream Products

• 78345-58-1 4-(cyclohexylamino)butanol 
• 6301-71-9 1-cyclohexyl-2,5-pyrrolidinedione 
• 717883-14-2 2,6-dicyclohexyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c′]dipyrrole-1,3,5,7(2H,6H)-tetrone 
• 1341207-40-6 3,3'-trisulphane-1,3-diylbis(4-chloro-1-cyclohexyl-1H-pyrrole-2,5-dione) 
• 41846-03-1 N¹,N⁴-dicyclohexylsuccinamide 

Relevant articles and documents

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Sepsis, a systemic inflammatory response, caused by pathogenic factors including microorganisms, has high mortality and limited therapeutic approaches. Herein, a new soluble epoxide hydrolase (sEH) inhibitor series comprising a phenyl ring connected to a

COMPOUND AND THERMOPLASTIC RESIN COMPOSITION AND MOLDED ARTICLE CONTAINING THE SAME

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Atypical oxidation reaction by thionyl chloride: Easy two-step synthesis of N-alkyl-1,4-dithiines

Easy two-step synthesis of a series of dithiines was performed from succinic anhydride via cyclization of the corresponding 4-(alkylamino)-4- oxobutanoic acids (succinamic acids). The reaction, carried out in polar aprotic solvents, gave 4,8-dithiine-indacene-1,3,5,7-tetraones (diimides 3) via 3,7-bis-4,8-dithia-indacene-1,5-diones (diisoimides 2), which could be isolated. Surprisingly, in this reaction, thionyl chloride appeared as an oxidant, and this process seemed to be useful for the syntheses of S-containing heterocyclic compounds such as 1,4-dithiins. A mechanistic pathway was considered. Copyright Taylor & Francis Group, LLC.