119030-72-7 Usage
Primary Use
Pharmaceutical intermediate
Derivative of
1,4-Butanediol (common industrial solvent and reagent)
Chemical Structure
Combination of phenyl and hydroxy moieties
Potential Applications
Synthesis of various drugs
Stereoisomeric Configuration
(2R,3R)(affects three-dimensional arrangement of functional groups)
Importance
Unique structural features hold promise for pharmaceutical research and development
Phenyl
Aromatic ring with delocalized electrons
Hydroxy
Contains an oxygen and hydrogen atom (-OH)
Methoxy
Oxygen and carbon atom connected to a hydrogen atom (-OCH3)
Acetate
A carboxylate functional group (-COO-) attached to a methyl group (-CH3)
Chirality
Presence of a chiral center (carbon atom with four different substituents) leading to stereoisomers
Enantiomers
Two stereoisomers that are mirror images of each other, but not superimposable (2R,3R)and (2S,3S)forms
Biological Interactions
Stereoisomeric configuration influences how the compound interacts with biological systems, such as enzymes and receptors
Solubility
Likely soluble in organic solvents due to its hydroxy and methoxy groups
Stability
May be sensitive to oxidation or hydrolysis due to the presence of phenolic hydroxy and ester groups
Synthesis
Can be synthesized through various chemical reactions, such as condensation, substitution, or reduction reactions
Purification
Techniques like chromatography or crystallization may be used to purify the compound from reaction mixtures
Check Digit Verification of cas no
The CAS Registry Mumber 119030-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,3 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119030-72:
(8*1)+(7*1)+(6*9)+(5*0)+(4*3)+(3*0)+(2*7)+(1*2)=97
97 % 10 = 7
So 119030-72-7 is a valid CAS Registry Number.
119030-72-7Relevant academic research and scientific papers
Oxidative Coupling of Lignans. IV. Monophenolic Oxidative Coupling
Burden, Jonathan K.,Cambie, Richard C.,Craw, Peter A.,Rutledge, Peter S.,Woodgate, Paul D.
, p. 919 - 933 (2007/10/02)
Oxidative coupling of the monophenolic monoester (6) gives an aryltetralin (12) which is a potential intermediate for the synthesis of clinically active monophenolic lignan lactones.In contrast, oxidative couplings of the monophenols (32) and (35), derived from matairesinol (29), give mixtures of diastereoisomeric cyclooctadiene lignans while 4'-demethyldeoxypodorhizon (26) does not cyclize.These results show that the degree of aromatic substitution in monophenolic diarylbutanes plays an important role in determining the outcome of oxidative coupling.An alternative synthesis of the lactone (57) from piperonal has been investigated.
