3089-25-6 Usage
Uses
Used in Polymer and Resin Synthesis:
2,4,4-trimethylhexane-1,6-diol is used as a monomer for the synthesis of various polymers and resins, such as polyurethane and polyester. Its unique structure and chemical properties contribute to the production of high-performance materials.
Used in Chemical Industry:
2,4,4-trimethylhexane-1,6-diol is used as a solvent and intermediate in the chemical industry. Its versatility allows it to be employed in a wide range of applications.
Used in Environmentally Friendly Applications:
2,4,4-trimethylhexane-1,6-diol is known for its low toxicity and environmentally friendly profile, making it a preferred choice for various industrial applications that prioritize sustainability and reduced environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 3089-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3089-25:
(6*3)+(5*0)+(4*8)+(3*9)+(2*2)+(1*5)=86
86 % 10 = 6
So 3089-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O2/c1-8(7-11)6-9(2,3)4-5-10/h8,10-11H,4-7H2,1-3H3
3089-25-6Relevant academic research and scientific papers
Lactones 34 [1]. Application of alcohol dehydrogenase from horse liver (HLADH) in enantioselective synthesis of δ- and ε-lactones
Boratynski, Filip,Kielbowicz, Grzegorz,Wawrzenczyk, Czeslaw
experimental part, p. 30 - 36 (2010/12/18)
The ability of horse liver alcohol dehydrogenase (HLADH) to the enantioselective oxidation of primary-primary, primary-secondary and primary-tertiary aliphatic 1,5- and 1,6-diols 1a-i was studied. No enantioselectivity of the transformations of primary-primary 1,6-diols 1a-d to ε-lactones 4a-d was observed. Regioselective oxidation of primary-secondary 1,6-diols 1e,f and 1,5-diols 1h,i afforded enantiomerically enriched ε-lactones 4e,f and δ-lactones 4h,i. ε-Lactones 4e,f were formed with higher enantiomeric excesses (e.e. = 85-99%). Enzymatic oxidation of primary-tertiary 1,6-diol 1g did not give lactone product.
