785015-46-5

Basic information

• Product Name: 3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)
• Synonyms: 3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)
• CAS NO: 785015-46-5
• Molecular Formula: C7H11NO2
• Molecular Weight: 0
• Product Categories: AMINOACID
• Mol File: 785015-46-5.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)(785015-46-5)
• EPA Substance Registry System: 3-Cyclohexene-1-carboxylicacid,2-amino-,(1R-trans)-(9CI)(785015-46-5)

Safety Data

• Hazardous Substances Data: 785015-46-5(Hazardous Substances Data)

Upstream product

• 123-51-3 i-Amyl alcohol 
• 118-92-3 anthranilic acid 
• 39170-51-9 7-azabicyclo[4.2.0]oct-4-en-8-one 
• 233600-33-4 rac,cis-2-(tert-butoxycarbonylamino)-cyclohex-3-ene carboxylic acid 
• 793634-65-8 2-amino-cyclohex-3-enecarboxylic acid ethyl ester 
• 1165952-91-9 cyclohexa-1,3-diene 
• 22031-53-4 cis-2-aza-3-oxobicyclo<4.2.0>octane 
• 285560-92-1 Butyric acid (1R,6S)-8-oxo-7-aza-bicyclo[4.2.0]oct-4-en-7-ylmethyl ester 
• 285560-95-4 (1S,6R)-7-hydroxymethyl-7-azabicyclo[4.2.0]oct-4-en-8-one 

Downstream Products

• 1378923-12-6 ethyl (1R,2R,3R,4R)-4-azido-2-(tert-butoxycarbonylamino)-3-hydroxycyclohexanecarboxylate 
• 1378923-13-7 ethyl (1R,2R,3S,4S)-3-azido-2-(tert-butoxycarbonylamino)-4-hydroxycyclohexanecarboxylate 

Relevant articles and documents

Stereo- and regiocontrolled syntheses of exomethylenic cyclohexane β-amino acid derivatives

Cyclohexane analogues of the antifungal icofungipen [(1R,2S)-2-amino-4-methylenecy clopentanecarboxylic acid] were selectively synthesized from unsaturated bicyclic β-lactams by transformation of the ring olefinic bond through three different regio- and s

Selective syntheses of novel highly functionalized β- aminocyclohexanecarboxylic acids

Highly functionalized β-aminocyclohexanecarboxylate regio- and stereoisomers were synthetized from racemic unsaturated bicyclic β-lactams via enzymatic resolution, selective transformation of the C-C double bond by stereoselective epoxidation, and regiose

Synthesis of orthogonally protected azepane β-amino ester enantiomers

A simple and convenient route is presented for the preparation of regio- and stereoisomers of novel azepane β-amino esters, starting from bicyclic β-lactam isomers. The synthetic procedure consists of dihydroxylation of the olefinic bond of the alicyclic amino esters, followed by NaIO4-mediated cleavage of the diol intermediate and reductive ring closure, which furnishes novel regioisomeric 5-aminoazepane-4-carboxylate and 3-aminoazepane-4-carboxylates. This method also allows the preparation of amino esters with an azepane skeleton in enantiomerically pure form.