13464-24-9 Usage
Description
4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE, also known as 2,4-Bis(4-hydroxyphenyl)-4-methyl-1-pentene, is an organic compound that serves as an intermediate in the synthesis of various chemical compounds. It is characterized by its unique molecular structure, which includes a 4-methylpent-1-ene backbone and two hydroxyphenyl groups attached at the 2,4 positions.
Uses
Used in Chemical Synthesis:
4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE is used as an intermediate in the synthesis of 4,4''-(1,3,3-Trimethyl-1-propene-1,3-diyl)bisphenol (T796655), a Bisphenol A (B519495) impurity with estrogenic activity. This intermediate plays a crucial role in the production of compounds with specific properties and applications in various industries.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of Bisphenol A impurities, 4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE contributes to the development of pharmaceutical compounds with potential therapeutic applications. The estrogenic activity of the synthesized compounds may have implications in the treatment of various health conditions related to hormonal balance.
Used in Research and Development:
4-METHYL-2,4-BIS(4-HYDROXYPHENYL)PENT-1-ENE is also utilized in research and development settings to explore its potential applications and properties. Scientists and researchers can use this intermediate to investigate its chemical behavior, reactivity, and possible uses in the synthesis of new compounds with unique characteristics and benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 13464-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13464-24:
(7*1)+(6*3)+(5*4)+(4*6)+(3*4)+(2*2)+(1*4)=89
89 % 10 = 9
So 13464-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H20O2/c1-13(14-4-8-16(19)9-5-14)12-18(2,3)15-6-10-17(20)11-7-15/h4-11,19-20H,1,12H2,2-3H3
13464-24-9Relevant articles and documents
Generation and synthetic uses of stable 4-[2-isopropylidene]-phenol carbocation from bisphenol A
Chen, Wei-Fu,Lin, Hsing-Yo,Dai, Shenghong A.
, p. 2341 - 2343 (2007/10/03)
(Equation Presented) Stable 4-[2-isopropylidene]-phenol carbocation, IPP cation 1, was generated readily by addition of bisphenol A in concentrated sulfuric acid at ambient temperature, and the cation could be used for facile syntheses of 4-isopropenyl phenol (IPP), IPP dimers, and spiro-bisphenol derivatives.