10468-32-3

Basic information

• Product Name: 3-Cyclohexene-1-acetic acid
• CAS NO: 10468-32-3
• Molecular Formula: C8H12O2
• Molecular Weight: 140.182
• Mol File: 10468-32-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Cyclohexene-1-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexene-1-acetic acid(10468-32-3)
• EPA Substance Registry System: 3-Cyclohexene-1-acetic acid(10468-32-3)

Safety Data

• Hazardous Substances Data: 10468-32-3(Hazardous Substances Data)

Upstream product

• 124-38-9 carbon dioxide 
• 2716-23-6 bicyclo[2.2.2]octan-2-one 
• 102369-51-7 (Cyclohexen-3-yl-1)-malonsaeure 
• 142607-97-4 2-Cyclohex-3-enylmethylene-[1,3]dithiane 
• 53631-80-4 ethyl 2-(cyclohex-3-en-1-yl)acetate 
• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 17138-28-2 (4-hydroxy-phenyl)-acetic acid ethyl ester 
• 106377-19-9 (Cyclohexen-3-yl-1)-malonsaeure-diethylester 
• 62141-22-4 2-(4-hydroxycyclohexyl)acetic acid ethyl ester 
• 34960-41-3 3-cyclohexenylbromomethane 
• 72581-32-9 cyclohex-3-enylmethanol 
• 18240-10-3 (+/-)-2-(3-cyclohexenyl)ethanol 

Downstream Products

• 111293-39-1 6-chloro-3-cyclohex-3-enylmethyl-1,1-dioxo-1,2(4)-dihydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 24476-16-2 1-(3'-cyclohexenyl)-2-propanone 
• 7086-71-7 3-cyclohexene-1-acetic acid chloride 
• 10468-33-4 2-(cyclohex-3-en-1-yl)acetamide 
• 61880-23-7 N-Methyl-3-cyclohexen-1-acetamid 
• 29927-52-4 Diazomethyl-cyclohexen-⁽³⁾-ylmethyl-keton 
• 76359-01-8 (cyclohex-3-en-1-ylmethyl)(phenylseleno)methanone 
• 18240-10-3 (+/-)-2-(3-cyclohexenyl)ethanol 
• 142608-00-2 5-(2-Methylamino-ethyl)-cyclohex-2-enol 
• 142607-99-6 2-(5-Hydroxy-cyclohex-3-enyl)-N-methyl-acetamide 
• 125422-13-1 2-methyl-2-azabicyclo<3.3.1>nonan-7α-yl 2,2-diphenylpropionate 
• 63540-01-2 2-(4-Cyclohexenyl)-ethylbromid 
• 52358-85-7 3-(3-Cyclohexen-1-yl)-3-buten-2-on 
• 52358-86-8 Methylspiro<2.5>oct-5-en-1-ylketon 

Relevant articles and documents

Catalytic Aza-Wacker Annulation: Tuning Mechanism by the Activation Mode of Amide and Enantioselective Syntheses of Melinonine-E and Strychnoxanthine

An unprecedented N-substituent of the amide was found to be crucial for the successful annulation to establish 2-azabicyclo[3.3.1]nonane and other ring skeletons in good yield. The novel catalytic aza-Wacker annulation methodology was further illustrated

A New Synthesis and Crystal Structure of 2-Methyl-2-azabicyclononan-7&α-ol

A facile, high yield synthesis of 2-methyl-2-azabicyclononan-7α-ol 2b from cyclohex-3-ene-1-carbaldehyde 3 is reported; an X-ray structure of 2b*HCl established the stereochemical assignment of 2b.