84189-13-9

Basic information

• Product Name: 1-Cyclohexene-1-acetyl chloride
• CAS NO: 84189-13-9
• Molecular Formula: C8H11ClO
• Molecular Weight: 158.628
• Mol File: 84189-13-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Cyclohexene-1-acetyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexene-1-acetyl chloride(84189-13-9)
• EPA Substance Registry System: 1-Cyclohexene-1-acetyl chloride(84189-13-9)

Safety Data

• Hazardous Substances Data: 84189-13-9(Hazardous Substances Data)

Upstream product

• 18294-87-6 1-cyclohexenylacetic acid 
• 14399-63-4 2-(1-hydroxycyclohexyl)acetic acid 
• 7719-09-7 thionyl chloride 
• 6975-71-9 1-cyclohexenylacetonitrile 

Downstream Products

• 27338-44-9 3-(cyclohex-1-en-1-yl)propionic acid 
• 768-50-3 1-cyclohexenylacetone 
• 4709-59-5 ethyl 2-(1-cyclohexenyl)acetate 
• 1017-23-8 2-(cyclohex-1-en-1-yl)-1-phenylethan-1-one 
• 99062-41-6 cyclohex-1-enyl-acetic acid methylamide 
• 119041-14-4 17-(2-cyclohex-1-enyl-ethyl)-morphinan-3-ol 
• 861310-40-9 1-cyclohex-1-enyl-butan-2-one 
• 88662-80-0 levonorgestrel cyclohexyl-1-enylacetate 
• 18938-05-1 (4R*,9S*,10S*)-tricyclo<8.4.0.0^4,9>tetradec-1(2)-en-3-one 
• 106476-87-3 1-(1-cyclohexenyl)-2-(1-cyclohexenyl)ethanone 
• 144709-79-5 1-(2-trimethylsilyl-2-cyclohexenyl)-2-(1-cyclohexenyl)ethanone 
• 144709-78-4 1-(2-cyclohexenyl)-2-(1-cyclohexenyl)ethanone 
• 156025-61-5 N-hydroxy-N-methyl-(1-cyclohexenyl)acetamide 
• 97387-52-5 [2-(2-Cyclohex-1-enyl-acetylamino)-phenyl]-propynoic acid methyl ester 

Relevant articles and documents

Practical asymmetric approach to medium-sized carbocycles based on the combination of two Ru-catalyzed transformations and a lewis acid-induced cyclization

(Chemical Equation Presented) Ruthenium-catalyzed coupling of allyl ethyl ether to optically active 1-trimethylsilyl-1-alkyn-3-ols, followed by in situ ketalization and Lewis-acid-induced cyclization, affords enantiomerically pure 1,5-oxygen-bridged eight

INTRAMOLECULAR DIELS-ALDER CYCLOADDITIONS OF VINYLKETENIMINES. A CONVERGENT ROUTE TO CARBAZOLES AND PYRIDOCARBAZOLE ALKALOIDS

The intramolecular Diels-Alder cycloaddition of acetylenic vinylketenimines is the key step of a highly convergent synthesis of carbazoles.A facile synthesis of N-methyl-tetrahydroellipticine has been completed in five isolated steps from N-methyl piperidone.

LONG-ACTING CONTRACEPTIVE AGENTS: LEVONORGESTREL ESTERS OF UNSATURATED ACIDS

Esters of levonorgestrel (13β-ethyl-17α-ethynyl-17β-hydroxygon-4-en-3-one) with a variety of unsaturated carboxylic acids have been synthesized for evaluation as potential long-acting, injectable contraceptive agents.