5438-66-4 Usage
Chemical Family
Alcohols
Structure
Phenylpropanoid with a benzyloxy group at the 4-position and a methoxy group at the 3-position
Functional Group
Propan-1-ol attached to the phenyl ring at the 1-position
Linear Carbon Chain
The propan-1-ol group creates a linear carbon chain
Applications
Organic synthesis and pharmaceutical research
Unique Structure
The specific arrangement of functional groups contributes to its potential biological activities
Biological Activities
Potential for various biological activities due to its unique structure
Derivation
Derived from a phenylpropanoid structure with additional functional groups
Molecular Weight
Approximately 312.4 g/mol (calculated from the molecular formula)
Check Digit Verification of cas no
The CAS Registry Mumber 5438-66-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5438-66:
(6*5)+(5*4)+(4*3)+(3*8)+(2*6)+(1*6)=104
104 % 10 = 4
So 5438-66-4 is a valid CAS Registry Number.
5438-66-4Relevant academic research and scientific papers
Efficient Total Synthesis of (±)-Isoguaiacin and (±)-Isogalbulin
Pilkington, Lisa I.,Song, Soo Min,Fedrizzi, Bruno,Barker, David
, p. 1449 - 1452 (2017/07/22)
1-Arylnaphthalene lignans such as (-)-isoguaiacin and (-)-isogalbulin have been reported to exhibit notable biological properties. While (-)-isoguaiacin has not been previously synthesized, syntheses of (-)-isogalbulin are generally long and produce a mixture of stereoisomers. We herein present the efficient total synthesis of (±)-isoguaiacin and (±)-isogalbulin in seven and eight steps with an overall yield of 46% and 36%, respectively. The reported approach harnesses a hydrogenolysis reaction in acidic conditions, to convert a furan into an arylnaphthalen structure.
