206990-79-6

Basic information

• Product Name: Carbonic acid (1R,6R)-1-[(1S,2S)-2,3-dihydroxy-1-(4-methoxy-benzyloxymethyl)-propyl]-8-hydroxy-6-methyl-nonyl ester methyl ester
• Synonyms: Carbonic acid (1R,6R)-1-[(1S,2S)-2,3-dihydroxy-1-(4-methoxy-benzyloxymethyl)-propyl]-8-hydroxy-6-methyl-nonyl ester methyl ester
• CAS NO: 206990-79-6
• Molecular Weight: 456.577
• Mol File: 206990-79-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbonic acid (1R,6R)-1-[(1S,2S)-2,3-dihydroxy-1-(4-methoxy-benzyloxymethyl)-propyl]-8-hydroxy-6-methyl-nonyl ester methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid (1R,6R)-1-[(1S,2S)-2,3-dihydroxy-1-(4-methoxy-benzyloxymethyl)-propyl]-8-hydroxy-6-methyl-nonyl ester methyl ester(206990-79-6)
• EPA Substance Registry System: Carbonic acid (1R,6R)-1-[(1S,2S)-2,3-dihydroxy-1-(4-methoxy-benzyloxymethyl)-propyl]-8-hydroxy-6-methyl-nonyl ester methyl ester(206990-79-6)

Safety Data

• Hazardous Substances Data: 206990-79-6(Hazardous Substances Data)

Upstream product

• 206990-68-3 (S)-4-[(1R,2S)-2-Benzyloxy-1-(4-methoxy-benzyloxymethyl)-but-3-ynyl]-2,2-dimethyl-[1,3]dioxolane 
• 206990-76-3 (S)-4-((1R,2S)-2-Benzyloxy-1-vinyl-but-3-ynyl)-2,2-dimethyl-[1,3]dioxolane 
• 206990-77-4 (2R,3S)-3-Benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-4-yn-1-ol 
• 206990-75-2 (3S,4R)-4-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hex-5-en-1-yn-3-ol 
• 206990-72-9 (R)-5-Hydroxy-3-methyl-pentanoic acid ethyl ester 
• 206990-66-1 (S)-5-Iodo-3-methyl-pentanoic acid ethyl ester 
• 206990-73-0 (S)-5-Iodo-3-methyl-pentanal 
• 206990-74-1 (S)-6-Iodo-4-methyl-hexan-2-ol 
• 117341-51-2 (3S,4R,4'S)-4-(2,2-dimethyl-1,3-dioxolan-4-yl)-1-(trimethylsilyl)-5-hexen-1-yn-3-ol 
• 72594-19-5 (R)-1-ethyl hydrogen-3-methylglutarate 

Downstream Products

• 206990-71-8 (2R,3R,8R)-2-(4-Methoxy-benzyloxymethyl)-3-methoxycarbonyloxy-8-methyl-10-oxo-undecanoic acid methyl ester 

Relevant articles and documents

A new synthetic approach to a fungal β-lactone based on the asymmetric [2,3]-wittig rearrangement

An asymmetric synthesis of the chiral β-lactone precursor of the HMG-CoA synthase, inhibitor L-659,699, is described, which involves as the key step an asymmetric [2,3]-Wittig rearrangement to control the stereogenic centers at the ring carbons (C2' and C