4486-59-3 Usage
General Description
2,6-Octadiene-4,5-diol, also known as octadienediol or 4,5-octadiene-1,2-diol, is a chemical compound with the molecular formula C8H14O2. It is a diol, meaning it contains two hydroxyl (OH) groups, and it is a colorless to pale yellow liquid. Octadienediol is used in the production of various polymers and resins, and it is also a versatile intermediate in the synthesis of other organic compounds. It can undergo reactions such as oxidation, acetylation, and esterification to yield a range of functionalized derivatives, making it useful in a variety of industrial applications. Additionally, octadienediol possesses antioxidant properties and is sometimes utilized in personal care products and cosmetics for its moisturizing and anti-aging effects. Overall, 2,6-octadiene-4,5-diol is a valuable compound in the chemical industry with a wide range of uses.
Check Digit Verification of cas no
The CAS Registry Mumber 4486-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4486-59:
(6*4)+(5*4)+(4*8)+(3*6)+(2*5)+(1*9)=113
113 % 10 = 3
So 4486-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-3-5-7(9)8(10)6-4-2/h3-10H,1-2H3
4486-59-3Relevant academic research and scientific papers
Selective Pinacol-Coupling Reaction using a Continuous Flow System
Sotto, Nicolas,Cazorla, Clément,Villette, Carole,Billamboz, Muriel,Len, Christophe
, p. 11065 - 11071 (2016/11/28)
The first continuous flow pinacol coupling reaction of carbonyl compounds was successfully achieved within only 2 min during a single pass through a cartridge filled with zinc(0). The optimized method allowed the efficient production of gram-scale value-added compounds with high productivity. The developed methodology is efficient for aromatic or α,β-unsaturated aldehydes but gives moderate results for more stable acetophenone derivatives. Moreover, the flow method displayed better results in terms of yield and selectivity in comparison to the corresponding batch methodology.
Selective Pinacol Coupling on Regeneratable Supported Acids in Sole Water
Sotto, Nicolas,Billamboz, Muriel,Chevrin-Villette, Carole,Len, Christophe
, p. 6375 - 6380 (2015/06/30)
Efficient pinacol coupling was developed in sole water, using a reusable heterogeneous supported acid source and zinc as cheap available metal source. This medium can be easily regenerated up to 10-fold without loss of activity. Moreover, supported acids enhance the selectivity of the pinacol coupling reaction compared with homogeneous acids.
