1437-81-6

Basic information

• Product Name: (+/-)-sulfuric acid mono-(cis-2-amino-cyclohexyl ester)
• CAS NO: 1437-81-6
• Molecular Weight: 195.24
• Mol File: 1437-81-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (+/-)-sulfuric acid mono-(cis-2-amino-cyclohexyl ester)(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-sulfuric acid mono-(cis-2-amino-cyclohexyl ester)(1437-81-6)
• EPA Substance Registry System: (+/-)-sulfuric acid mono-(cis-2-amino-cyclohexyl ester)(1437-81-6)

Safety Data

• Hazardous Substances Data: 1437-81-6(Hazardous Substances Data)

Upstream product

• 6850-38-0 2-aminocyclohexanol 
• 931-16-8 (+/-)-trans-2-aminocyclohexanol 
• 286-20-4 cyclohexane-1,2-epoxide 
• 38898-70-3 cis-2-amino-cyclohexanol-⁽¹⁾ 

Downstream Products

• 108-94-1 cyclohexanone 
• 117864-55-8 N-[2-(7-aza-norcaran-7-yl)-cyclohexyl]-benzamide 
• 931-12-4 trans-2-chloro-cyclohexylamine 
• 29558-85-8 7-aza-norcarane-7-carbothioic acid anilide 
• 10514-92-8 trans-2-amino-1-cyclohexanethiol 
• 100385-40-8 optically inactive bis-(trans-2-amino-cyclohexyl)-disulfide 

Relevant articles and documents

Synthesis and spectral properties of N sulfated and/or O sulfated amino alcohols

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Convenient Approach to 2-Substituted (Thio)morpholin-3-ones from α-Diazoacetates via X-H Carbene Insertion – Lactamization Sequence

Stepwise coupling of N-Boc-protected β-aminoethanols or β-mercaptoethylamines with various α-diazoacetates provides a new, unified approach to constructing (thio)morpholin-3-ones. The process involves a Rh2(esp)2-catalyzed X-H insert

A versatile synthesis of various substituted taurines from vicinal amino alcohols and aziridines

Taurine and structurally diverse substituted taurines have been synthesized by peroxyformic acid, oxidation of the thiazolidine-2-thione intermediates generated from, vicinal amino alcohols or aziridines and carbon disulfide. The stereochemistry and mechanisms of the reactions are disscussed. The method is a salt-free and versatile route, convenient in terms of purification, and can be used to synthesize optically active substituted taurines.