512791-23-0

Basic information

• Product Name: Bicyclo[2.2.1]hept-5-ene-2-methanol, 3-[(methoxymethoxy)methyl]-, (1R,2S,3R,4S)-rel- (9CI)
• Synonyms: Bicyclo[2.2.1]hept-5-ene-2-methanol, 3-[(methoxymethoxy)methyl]-, (1R,2S,3R,4S)-rel- (9CI)
• CAS NO: 512791-23-0
• Molecular Formula: C11H18O3
• Molecular Weight: 198.25882
• Product Categories: CYCLOPENTANE
• Mol File: 512791-23-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bicyclo[2.2.1]hept-5-ene-2-methanol, 3-[(methoxymethoxy)methyl]-, (1R,2S,3R,4S)-rel- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Bicyclo[2.2.1]hept-5-ene-2-methanol, 3-[(methoxymethoxy)methyl]-, (1R,2S,3R,4S)-rel- (9CI)(512791-23-0)
• EPA Substance Registry System: Bicyclo[2.2.1]hept-5-ene-2-methanol, 3-[(methoxymethoxy)methyl]-, (1R,2S,3R,4S)-rel- (9CI)(512791-23-0)

Safety Data

• Hazardous Substances Data: 512791-23-0(Hazardous Substances Data)

Upstream product

• 941567-71-1 (1R,2S,3R,4S)-bicyclo[2.2.1]hept-5-ene-2,3-dimethanol 
• 107-30-2 chloromethyl methyl ether 
• 131694-93-4 (-)-methyl (1R,4S)-3-endo-<(methoxymethoxy)methyl>bicyclo<2.2.1>hept-5-ene-2-endo-carboxylate 
• 131726-11-9 (2,S)-endo-methoxycarbonyl-(3,R)-endo-hydroxymethylbicyclo<2.2.1>heptene-5 

Downstream Products

• 512791-31-0 (3-vinylbicyclo[2.2.1]hept-5-en-2-yl)methan-1-ol 
• 512791-35-4 3-vinylbicyclo[2.2.1]hept-5-ene-2-carbaldehyde 

Relevant articles and documents

Synthetic studies on Diels-Alder adducts: Intramolecular interactions between two functions

In this paper we describe the synthesis of a ?,?-unsaturated aldehyde from a bicyclic Diels-Alder adduct, to be used in future electrocyclic reaction studies. A number of reactions produced undesired materials resulting from the interaction between functions, forcing the use of partial protection to accomplish a synthesis that would be otherwise straightforward. Suggestions to account for the results are given.

Novel Route to Some Biologically Important Compounds Starting with a Common Chiral, Bicyclic, Fused Lactone: Enantioselective Synthesis of (-)-Boschnialactone and Two Antithrombotics

Three biologically important compounds, (-)-boschnialactone and the antithrombotics (+)- and (-)-(5Z)-6-hept-5-en-2-endo- and exo-yl>hex-5-enoic acid have been synthesized starting from a common

Enantioselective Synthesis of (-)-Boschnialactone

An enantioselective synthesis of (-)-boschnialactone was accomplished starting from a chiral fused bicycloheptane lactone readily available via an asymmetric Diels-Alder reaction.