1026090-92-5

Basic information

• Product Name: (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide
• Synonyms: (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide
• CAS NO: 1026090-92-5
• Molecular Weight: 269.384
• Mol File: 1026090-92-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide(1026090-92-5)
• EPA Substance Registry System: (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide(1026090-92-5)

Safety Data

• Hazardous Substances Data: 1026090-92-5(Hazardous Substances Data)

Upstream product

• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 1027079-96-4 (4aR,8R,8aR)-8-isopropyl-5-methyl-1,4,4a,7,8,8a-hexahydroisochromen-3-one 

Downstream Products

• 1025963-57-8 (1R,5R,6R)-2-(5-isopropyl-2-methyl-6-vinylcyclohex-2-enyl)-N-methoxy-N-methylacetamide 
• 1028264-59-6 (1R,5R,6R)-(5-isopropyl-2-methyl-6-vinylcyclohex-2-enyl)acetic acid 
• 1026388-98-6 (1R,5R,6R)-(5-isopropyl-2-methyl-6-vinylcyclohex-2-enyl)acetaldehyde 
• 198336-00-4 (1R,5R,6R)-2-[6-(tert-butyldimethylsilanyloxymethyl)-5-isopropyl-2-methylcyclohex-2-enyl]acetaldehyde 
• 1026860-41-2 (1R,5R,6R)-2-(6-formyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-methylacetamide 
• 1027570-52-0 (1R,5R,6R)-2-(5-isopropyl-2-methyl-6-triethylsilanyloxymethylcyclohex-2-enyl)-N-methoxy-N-methylacetamide 
• 1028292-30-9 (1R,5R,6R)-2-[6-(tert-butyldimethylsilanyloxymethyl)-5-isopropyl-2-methylcyclohex-2-enyl]-N-methoxy-N-methylacetamide 

Relevant articles and documents

A convergent approach to the marine natural product eleutherobin: Synthesis of key intermediates and attempts to produce the basic skeleton

Synthesis of (1R,5R,6R)-2-(6-hydroxymethyl-5-isopropyl-2-methylcyclohex-2-enyl)-N-methoxy-N-m ethylacetamide 8 from R-(-)-phellandrene in six steps, and (3aR*,4S*,6R*,6aS*)-(6-hydroxymethyl-4-methoxy-2,2,6-tri methyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)acetic acid methyl ester 17 from tetrabromoacetone and 2-methoxy-5-methyl-furan in six steps, provided two key fragments which have been combined to produce intermediates for attempted construction of the basic skeleton of eleutherobin.