132392-28-0 Usage
Uses
Used in Organic Synthesis:
2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE is used as a building block in organic synthesis for the preparation of complex molecules. Its unique structure and reactivity make it a valuable component in the creation of advanced organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE is used as a research compound for the development of new drugs. Its structural features and reactivity may contribute to the discovery of novel therapeutic agents.
Used in Agrochemical Development:
2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE is also utilized in the agrochemical sector for the development of new pesticides or other agricultural chemicals. Its properties may offer innovative solutions for crop protection and management.
Used in Materials Science:
In the field of materials science, 2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE is used for the research and development of new materials with specific properties. Its unique structure may contribute to the creation of advanced materials with applications in various industries.
Safety Precautions:
It is important to handle 2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE with caution, as it is a potentially hazardous chemical. Proper safety measures should be taken during its use to minimize risks to health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 132392-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,9 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132392-28:
(8*1)+(7*3)+(6*2)+(5*3)+(4*9)+(3*2)+(2*2)+(1*8)=110
110 % 10 = 0
So 132392-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H21BrO/c1-15(2)7-8-16(3,4)13-9-11(14(18)10-17)5-6-12(13)15/h5-6,9H,7-8,10H2,1-4H3
132392-28-0Relevant articles and documents
Synthesis and biological activities of new heterocyclic aromatic retinoids
Diaz,Michel,Stella,Charpentier
, p. 2289 - 2294 (2007/10/03)
A series of 3-aryl-2H-1-benzopyrancarboxylic acid derivatives was synthesized and evaluated as Retinoic Acid Receptor (RAR) agonists. By modifications of the 3-aryl group, we have obtained new retinoids exhibiting potent cellular differentiating activities and high affinities for RARs. Moreover, hydrogenation of the 2H-1-benzopyran ring led to the 3-(5,6,7,8-tetrahydro-5,5,8,8,-tetramethyl -naphthalen-2-yl)-3,4-dihydro-2H-1-benzopyran-7-yl carboxylic acid, characterized by a RARβ binding profile.
