66818-21-1 Usage
Description
1,5-Decalindiol, also known as decalin-1,5-diol, is a synthetic chemical compound with the molecular formula C10H18O2. It is a diol, meaning it contains two hydroxyl (OH) groups. 1,5-DECALINDIOL is commonly used as a precursor for the synthesis of various pharmaceuticals and biologically active compounds. Additionally, it is utilized in the production of fragrance and flavoring agents. Due to its combustible nature and potential to cause skin and eye irritation, respiratory issues, and allergic reactions, proper handling and precautionary measures should be taken when working with 1,5-decalindiol.
Uses
Used in Pharmaceutical Industry:
1,5-Decalindiol is used as a precursor for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and functional groups make it a valuable building block in the development of new drugs and therapeutic agents.
Used in Fragrance and Flavoring Industry:
1,5-Decalindiol is used as a component in the production of fragrance and flavoring agents. Its chemical properties allow it to contribute to the creation of unique scents and tastes in various consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 66818-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,1 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66818-21:
(7*6)+(6*6)+(5*8)+(4*1)+(3*8)+(2*2)+(1*1)=151
151 % 10 = 1
So 66818-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h7-12H,1-6H2
66818-21-1Relevant articles and documents
Synthesis of 3,4,7,8-tetrahydronaphthalene-1,5(2H,6H)-dione
Minne, Garrett B.,De Clercq, Pierre J.
, p. 183 - 187 (2007/10/03)
A short and high yielding route for the preparation of the title compound, starting from commercially available 1,5-dihydroxynaphthalene, is described. The key step in the sequence is the air oxidation of a bis(trimethylsilyloxy)diene precursor.