1252823-49-6 Usage
Molecular Weight
257.32 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
Dibenzofuranol ring with a hexahydro-3-methyl group The structure of the compound is characterized by a dibenzofuranol ring, which is a six-membered ring containing oxygen and benzene rings, and a hexahydro-3-methyl group, which is a six-carbon alkyl group with a methyl substituent.
Cyclic Compound
Yes The compound is a cyclic compound, meaning it has a ring structure.
Aromatic
Yes The compound is aromatic, meaning it has a stable, delocalized electron system in its benzene rings.
Polarity
Low The compound has low polarity due to the nonpolar nature of the hexahydro-3-methyl group.
Solubility
Insoluble in water, soluble in organic solvents The compound is insoluble in water due to its nonpolar nature but can dissolve in organic solvents such as ethanol or methanol.
Uses
Building block in the synthesis of other organic compounds, pharmaceutical research The compound is used as a building block in the synthesis of other organic compounds and in pharmaceutical research. Its specific applications depend on its structure and reactivity in different chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1252823-49-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,2,8,2 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1252823-49:
(9*1)+(8*2)+(7*5)+(6*2)+(5*8)+(4*2)+(3*3)+(2*4)+(1*9)=146
146 % 10 = 6
So 1252823-49-6 is a valid CAS Registry Number.
1252823-49-6Relevant articles and documents
Synthesis and inhibitory evaluation of cyclohexen-2-yl- and cyclohexyl-substituted phenols and quinones to endothelial cell and cancer cells
Liu, Xin,Ou, Yingyong,Chen, Shaopeng,Lu, Xin,Cheng, Hao,Jia, Xian,Wang, Decai,Zhou, Guo-Chun
experimental part, p. 2147 - 2153 (2010/07/04)
Alkylation of phenols with 1,3-cyclohexadiene (1) has been conducted and a series of cyclohexen-2-yl- and cyclohexyl-substituted phenols and quinones were screened against the proliferation of HUVEC and cancer cells. Phenol type as well as the size and occupied position of the substitute are important for the alkylating reaction and the inhibitory activity and selectivity of a compound. 2,5-Di(cyclohexen-2-yl)benzene-1,4-diol (25) bearing two cyclohexen-2-yl groups and 2-tert-butyl-5-(cyclohexen-2-yl)benzene-1,4-diol (30) bearing cyclohexen-2-yl and tert-butyl groups exhibited good selectivity against HUVEC proliferation (IC50s of 2.0 and 1.4?μM, respectively) with relatively low toxicity to ccc-HPF-1.
