112996-29-9 Usage
Molecular structure
A complex and unique structure containing an oxaspiro ring, a hydroxy group, and a phenyl group with a propenyloxy substituent.
Hydroxy group
A polar functional group (-OH) that can participate in hydrogen bonding and affect the compound's solubility and reactivity.
Phenyl group
A benzene ring with delocalized electrons, providing aromaticity and potential sites for further functionalization.
Propenyloxy substituent
A three-carbon alkenyl chain with an ether oxygen atom attached to the phenyl group, influencing the compound's reactivity and physical properties.
Chemical properties
The compound may exhibit various chemical properties due to its distinct structure, such as reactivity with other chemicals or the ability to form derivatives.
Biological properties
The compound may have potential biological activities, making it of interest for pharmaceutical applications or research.
Potential applications
Due to its unique structure and properties, the compound could be of interest for use in pharmaceuticals, materials, or other industries.
Further research
More investigation and research are needed to fully understand the compound's potential uses, effects, and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 112996-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112996-29:
(8*1)+(7*1)+(6*2)+(5*9)+(4*9)+(3*6)+(2*2)+(1*9)=139
139 % 10 = 9
So 112996-29-9 is a valid CAS Registry Number.
112996-29-9Relevant articles and documents
An Approach for General Synthesis of Biphenyl Neolignans by the Reaction of 1-Oxaspirodeca-6,9-diene-2,8-dione with the Grignard Reagent and Synthesis of Magnaldehyde B
Takeya, Tetsuya,Okubo, Toru,Tobinaga, Seisho
, p. 1755 - 1761 (2007/10/02)
An approach for general synthesis of biphenyl neolignans by the reactionof 1-oxaspiro-deca -6,9-diene-2,8-dione (3) (quinol-lactone) with the Grignard reagent 4 was explored.Among the biphenyl derivatives 6,8 and 9 thus obtained, 6 was transformed to magnaldehyde B (2b) in three steps.Keywords---biphenyl neolignan; synthesis; magnaldehyde B; quinol-lactone; Grignard reagent
