104561-41-3 Usage
Description
4-[2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)ethynyl)-benzoic acid is a complex organic compound characterized by its unique molecular structure. It is a derivative of benzoic acid with an ethynyl group attached to the 2nd position of a naphthalene ring, which is further substituted with methyl groups and part of a tetrahydro structure. 4-[2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)ethynyl)-benzoicacid holds potential for various applications due to its structural properties and interactions with other molecules.
Uses
Used in Pharmaceutical Industry:
4-[2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)ethynyl)-benzoic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to serve as a building block for the development of new drugs targeting specific biological pathways.
Used in Chemical Research:
In the field of chemical research, this compound can be used as a research tool to study the effects of structural modifications on the properties and reactivity of naphthalene-based molecules. It can provide insights into the design of new molecules with tailored characteristics for different applications.
Used in Material Science:
4-[2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)ethynyl)-benzoic acid may also find applications in material science, potentially being used in the development of novel materials with specific optical, electronic, or mechanical properties due to its rigid and planar structure.
Used in the Synthesis of Advanced Materials:
Given its structural complexity, this compound could be utilized in the synthesis of advanced materials such as organic semiconductors, photovoltaic cells, or light-emitting diodes (OLEDs) where its electronic properties could be advantageous.
It is important to note that the specific applications of 4-[2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)ethynyl)-benzoic acid would depend on further research and development to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 104561-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104561-41:
(8*1)+(7*0)+(6*4)+(5*5)+(4*6)+(3*1)+(2*4)+(1*1)=93
93 % 10 = 3
So 104561-41-3 is a valid CAS Registry Number.
104561-41-3Relevant articles and documents
Retinoid compounds and their use
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, (2012/11/06)
The invention relates to retinoid compounds of the formula (I): wherein V is a hydrophobic group;W is a non-polyenic linker; andX is a polar group comprising a hydrogen bond donor; or a salt thereof, and to the use of such compounds in the control of cell differentiation.
Synthesis and evaluation of synthetic retinoid derivatives as inducers of stem cell differentiation
Christie, Victoria B.,Barnard, Jonathan H.,Batsanov, Andrei S.,Bridgens, Caroline E.,Cartmell, Emily B.,Collings, Jonathan C.,Maltman, Daniel J.,Redfern, Christopher P. F.,Marder, Todd B.,Przyborski, Stefan,Whiting, Andrew
scheme or table, p. 3497 - 3507 (2009/02/05)
All-trans-retinoic acid (ATRA) and its associated analogues are important mediators of cell differentiation and function during the development of the nervous system. It is well known that ATRA can induce the differentiation of neural tissues from human pluripotent stem cells. However, it is not always appreciated that ATRA is highly susceptible to isomerisation when in solution, which can influence the effective concentration of ATRA and subsequently its biological activity. To address this source of variability, synthetic retinoid analogues have been designed and synthesised that retain stability during use and maintain biological function in comparison to ATRA. It is also shown that subtle modifications to the structure of the synthetic retinoid compound impacts significantly on biological activity, as when exposed to cultured human pluripotent stem cells, synthetic retinoid 4-(5,5,8,8-tetramethyl-5,6,7,8- tetrahydronaphthalen-2-ylethynyl)benzoic acid, 4a (para-isomer), induces neural differentiation similarly to ATRA. In contrast, stem cells exposed to synthetic retinoid 3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylethynyl)benzoic acid, 4b (meta-isomer), produce very few neurons and large numbers of epithelial-like cells. This type of structure-activity-relationship information for such synthetic retinoid compounds will further the ability to design more targeted systems capable of mediating robust and reproducible tissue differentiation.
Diarylacetylenes and their use in treating acne
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, (2008/06/13)
Novel diarylacetylenes of the formula I STR1 where A, R1, R2, R3, R4, R5 and R6 have the meanings stated in the description, are useful for the treatment of dermatological disorders.
