108898-22-2

Basic information

• Product Name: 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl chloride
• Synonyms: 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl chloride
• CAS NO: 108898-22-2
• Molecular Weight: 252.784
• Mol File: 108898-22-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl chloride(108898-22-2)
• EPA Substance Registry System: 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl chloride(108898-22-2)

Safety Data

• Hazardous Substances Data: 108898-22-2(Hazardous Substances Data)

Upstream product

• 5300-00-5 (2E,4E)-3-Methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienoic acid methyl ester 
• 79-77-6 (E)-β-ionone 
• 14398-42-6 (2E,4E)-3-methyl-5-(2,6,6-trimethylcyclohex-1-enyl)penta-2,4-dienoic acid 

Downstream Products

• 102658-36-6 4-[3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoyl]-morpholine 
• 212118-26-8 3-Methoxy-4-[(2E,4E)-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienoylamino]-benzoic acid 2-trimethylsilanyl-ethyl ester 
• 212118-27-9 4-{Methyl-[(2E,4E)-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienoyl]-amino}-benzoic acid 2-trimethylsilanyl-ethyl ester 
• 212118-25-7 4-[(2E,4E)-3-Methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-dienoylamino]-benzoic acid 2-trimethylsilanyl-ethyl ester 
• 102707-95-9 3-methyl-5t-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2t,4-dienoic acid diethylamide 

Relevant articles and documents

A rapid, mild and acid-free procedure for the preparation of acyl chlorides including formyl chloride

Carboxylic acids are converted by hexachloroacetone and triphenylphosphine at -78°C in methylene chloride to the corresponding acyl chlorides. Formic acid can be used to generate formyl chloride at -78°C in order to perform formylation under very mild conditions.

Synthesis and structure-activity relationships of 2- pyrazinylcarboxamidobenzoates and β-ionylideneacetamidobenzoates with retinoidal activity

The structure-activity relationships of two series of novel retinoids (2-pyrazinylcarboxamidobenzoates and β-ionylideneacetamidobenzoates) have been investigated by evaluating their ability to induce differentiation in both human promyelocytic leukemia (H