98235-76-8 Usage
Uses
Used in Pharmaceutical Industry:
Cis-6,7-dihydroxy-5,6,7,8-tetrahydronaphthalen-1-yl acetate is used as an active pharmaceutical ingredient for the development of certain medications. Its hydroxyl and acetyl groups contribute to its bioactivity and potential therapeutic effects, making it a promising candidate for drug discovery and formulation.
Used in Perfumery:
In the perfume industry, Cis-6,7-dihydroxy-5,6,7,8-tetrahydronaphthalen-1-yl acetate is used as a fragrance ingredient. Its unique scent profile and stability make it a valuable component in creating various perfumes and fragrances.
Used as a Precursor in Chemical Synthesis:
Cis-6,7-dihydroxy-5,6,7,8-tetrahydronaphthalen-1-yl acetate serves as a precursor in the synthesis of other chemical compounds. Its reactivity and functional groups facilitate its use in the production of a range of chemicals, contributing to the diversity of organic chemistry.
Used in Chemical Research and Development:
Due to its unique structure and properties, Cis-6,7-dihydroxy-5,6,7,8-tetrahydronaphthalen-1-yl acetate is employed in chemical research for exploring new reactions, synthesis pathways, and potential applications. Its versatility and adaptability make it an essential tool for advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 98235-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,3 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98235-76:
(7*9)+(6*8)+(5*2)+(4*3)+(3*5)+(2*7)+(1*6)=168
168 % 10 = 8
So 98235-76-8 is a valid CAS Registry Number.
98235-76-8Relevant academic research and scientific papers
Enantioselective synthesis of the individual stereoisomers of a brassinolide mimetic
Back, Thomas G.,Bey, Michael A.,Parvez, Masood,Pharis, Richard P.
, p. 873 - 880 (2007/10/03)
The syntheses of all four stereoisomers of a nonsteroidal mimetic of the phytohormone brassinolide are reported. These are: (+)-(6S,7R,6′S, 7′)-, (-)-(6R,7S,6′R,7′)-, (+)-(6S,7R,6′R,7′)-, and (-)-(6R,7S,6′S,7′R)-1-[1-(4,6,7-trihydroxy-5,6,7,8- tetrahydron
