92822-62-3

Basic information

• Product Name: 2,3-O-cyclohexylidene-D,L-glyceraldehyde
• CAS NO: 92822-62-3
• Molecular Weight: 170.208
• Mol File: 92822-62-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2,3-O-cyclohexylidene-D,L-glyceraldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-O-cyclohexylidene-D,L-glyceraldehyde(92822-62-3)
• EPA Substance Registry System: 2,3-O-cyclohexylidene-D,L-glyceraldehyde(92822-62-3)

Safety Data

• Hazardous Substances Data: 92822-62-3(Hazardous Substances Data)

Usage

Chemical Compound

2,3-O-cyclohexylidene-D,L-glyceraldehyde

Derivation

Derived from D,L-glyceraldehyde

Functional Group

Contains a cyclohexylidene group

Attachment

Attached to the 2 and 3 carbon atoms

Usage

Organic Synthesis: Commonly used in organic synthesis
Building Block: Primarily used as a building block in the preparation of various organic molecules and pharmaceuticals
Synthesis of Natural Products: Utilized in the synthesis of complex natural products
Reagent: Used as a reagent in stereoselective reactions
Development of New Materials: Applications in the development of new materials
Carbohydrate Chemistry and Biochemistry: Valued for its role in the study of carbohydrate chemistry and biochemistry

Upstream product

• 99744-80-6 4,5-O-cyclohexylidene-L-arabinose dibenzyl dithioacetal 
• 102335-37-5 5-((2S)-1,4-dioxaspiro[4.5]dec-2-yl)(3S,4R,5S)-3,4-dihydroxy-3,4,5-trihydrofuran-2-one 
• 108-94-1 cyclohexanone 
• 103959-91-7 (S)-2-(benzyloxy)-2-{(S)-1',4'-dioxaspiro[4.5]decan-2'-yl}ethan-1-ol 
• 76779-67-4 1,2,5,6-di-O-cyclohexylidene-D-mannitol 
• 881377-27-1 5,6-O-cyclohexylidene-gulono-1,4-lactone 
• 229639-21-8 3,4-O-cyclohexylidene-L-(S)-erythrulose 
• 933-40-4 cycloxexanone dimethyl ketal 
• 229639-27-4 (S)-1-(1,4-Dioxa-spiro[4.5]dec-2-yl)-ethane-1,2-diol 
• 6614-52-4 5,6-O-cycloheyxlidene-(L)-ascorbic acid 

Downstream Products

• 1193305-57-5 dibenzyl (1S,2R)-2,3-O-cyclohexylidene-1,2,3-trihydroxypropylphosphonate 
• 1193305-51-9 dibenzyl (1R,2R)-2,3-O-cyclohexylidene-1,2,3-trihydroxypropylphosphonate 
• 116185-65-0 (1R,2R,S,4R)-5-(benzyloxy)-1-(2,2-pentamethylene-1,3-dioxolan-4-yl)-4-methylpentan-2-ol 
• 82372-20-1 (1,4-dioxaspiro[4.5]decan-2-yl)methyl benzoate 
• 1359850-02-4 C₂₈H₂₆O₅ 
• 308795-21-3 (2S,4R,5S)-1,2-O-cyclohexylidene-1,2,5-trihydroxy-5-cyclohexyl-4-methylheptan-3-one 
• 308795-23-5 (2S,4R,5R)-1,2-O-cyclohexylidene-1,2,5-trihydroxy-4-methyl-5-(4-chlorophenyl)pentan-3-one 
• 308795-22-4 (2S,4R,5R)-1,2-O-cyclohexylidene-1,2,5-trihydroxy-4-methyl-5-phenylpentan-3-one 
• 609-06-3 L-xylose 
• 1949-78-6 L-lyxose 
• 24259-59-4 L-ribose 
• 5328-37-0 L-arabinose 

Relevant articles and documents

Synthesis and in vitro biological evaluation of 3-amino-3-deoxydihydrosphingosines and their analogues

The stereoselective synthesis of the 3-amino-3-deoxydihydrosphingosines and their isomeric analogues from dimethyl L-tartrate is described by means of [3,3]-sigmatropic rearrangements and the cross metathesis reaction as a cornerstone of the developed str

Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragment

The enantioselective total synthesis of callipeltoside A is described. Two syntheses of the macrolactone subunit are included: the first relies upon an Ireland-Claisen rearrangement to generate the trisubstituted olefin geometry and the second utilizes an enantioselective vinylogous aldol reaction for this purpose. Enantioselective syntheses of the sugar and chlorocyclopropane side chain fragments are also disclosed. The relative and absolute stereochemistry of this natural product was determined by fragment coupling with the two enantiomers of the side chain fragment.

EXPEDITIOUS SYNTHESIS OF DPD

This invention provides a practical synthesis route for 4,5-dihydroxypentane-2,3-dione (DPD), an unstable small molecule which is proposed to be the source of universal signaling agents for quorum sensing in bacteria. The synthesis route includes new intermediates and allows preparation of isotopically-labeled DPD and ent-DPD. The method provides sufficient quantities of DPD for study of spontaneous binding of borate to DPD, the signal for the marine bacteria V. harveyi