84011-70-1

Basic information

• Product Name: 1-oxo-5-hydroxy-methyl-2-cyclohexene
• Synonyms: 1-oxo-5-hydroxy-methyl-2-cyclohexene
• CAS NO: 84011-70-1
• Molecular Weight: 126.155
• Mol File: 84011-70-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-oxo-5-hydroxy-methyl-2-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-oxo-5-hydroxy-methyl-2-cyclohexene(84011-70-1)
• EPA Substance Registry System: 1-oxo-5-hydroxy-methyl-2-cyclohexene(84011-70-1)

Safety Data

• Hazardous Substances Data: 84011-70-1(Hazardous Substances Data)

Upstream product

• 63723-94-4 3-ethoxy-5-carbethoxy-2-cyclohexenone 
• 201230-82-2 carbon monoxide 
• 15135-97-4 (trans-2-vinylcyclopropyl)methanol 
• 15135-97-4 <2-ethenylcyclopropyl>methanol 
• 4720-83-6 6-oxabicyclo[3.2.1]oct-3-en-7-one 
• 24941-58-0 3,5-dimethoxycyclohexa-2,5-diene-1-carboxylic acid 
• 90612-16-1 (3,5-dimethoxycyclohexa-2,5-dien-1-yl)methanol 
• 70150-59-3 1-Hydroxy-3-oxo-5-hydroxymethyl-cyclohexen 
• 947623-53-2 C₉H₁₄O₃ 
• 118-41-2 Eudesmic acid 
• 156041-33-7 5-hydroxymethylcyclohex-2-en-1-ol 
• 42858-60-6 3,5-cyclohexanedione-1-carboxylic acid 

Downstream Products

• 947623-54-3 C₁₅H₁₈O₃ 
• 539-80-0 Tropone 
• 1901-34-4 cyclohepta-2,4-dienone 
• 1166841-87-7 acetic acid (S)-5-oxo-cyclohex-3-enylmethyl ester 
• 155751-23-8 (R)-5-(hydroxymethyl)-2-cyclohexen-1-one 
• 113452-39-4 5-acetoxymethylcyclohex-2-en-1-one 

Relevant articles and documents

Divergent Total Syntheses of (?)-Huperzine Q, (+)-Lycopladine B, (+)-Lycopladine C, and (?)-4-epi-Lycopladine D

We report herein our synthetic efforts towards the divergent syntheses of (?)-huperzine Q (1), (+)-lycopladine B (2), (+)-lycopladine C (3), and (?)-lycopladine D (4). The 10-step total synthesis of (?)-huperzine Q (1) and the first total syntheses of (+)

Total syntheses of (-)-huperzine Q and (+)-lycopladines B and C

Utilizing a late-stage enamine bromofunctionalization strategy, the twelve-step total synthesis of (-)-huperzine Q was accomplished. Furthermore, the first total syntheses of (+)-lycopladines B and C are described. An unprecedented X-ray crystal structure

Asymmetric synthesis of palitantin by an enzymatic and organocatalytic approach

The natural enantiomer of the fungal metabolite (+)-palitantin has been synthesized by adopting a chemoenzymatic and organocatalytic approach. Lipase catalyzed kinetic resolution, Sharpless asymmetric dihydroxylation and organocatalytic asymmetric hydroxy