1,1-Bis(1-methylethoxy)cyclohexane
Acetals and hemiacetals, whether or not with other oxygen function, and their halogenated, sulfonated, nitrated or nitrosated derivatives: > 1,1-Bis(1-methylethoxy)cyclohexane
Duty Rate (from China)
Except for products described in headings 9903.03.02–9903.03.11, articles the product of any country, as provided for in subdivision (aa) of U.S. note 2 to this subchapter
Except as provided in headings 9903.88.13, 9903.88.18, 9903.88.33, 9903.88.34, 9903.88.35, 9903.88.36, 9903.88.37, 9903.88.38, 9903.88.40, 9903.88.41, 9903.88.43, 9903.88.45, 9903.88.46, 9903.88.48, 9903.88.56, 9903.88.64, 9903.88.66, 9903.88.67, 9903.88.68, or 9903.88.69, articles the product of China, as provided for in U.S. note 20(e) to this subchapter and as provided for in the subheadings enumerated in U.S. note 20(f)
Products classified under HTS 2911.00.10.00
1,1-Bis(1-methylethoxy)cyclohexane
1,1-Bis(1-methylethoxy)cyclohexane is a specific acetal compound featuring a cyclohexane ring with two isopropoxy groups attached to the same carbon, classified under HTS 2911.00.10.00 as an acetal with oxygen function. It serves as a chemical intermediate in organic synthesis, particularly for protecting carbonyl groups in pharmaceutical and agrochemical production.
1,1-Diisopropoxy Cyclohexane Technical Grade
Technical grade 1,1-bis(1-methylethoxy)cyclohexane (>98% purity) used in lab-scale organic protection reactions. Falls squarely under HTS 2911.00.10.00 as the named acetal compound per subheading specificity. Commonly employed in multi-step synthesis of complex pharmaceuticals.
Cyclohexane Bis(Isopropyl Acetyl) 99% Pure
High-purity 1,1-bis(1-methylethoxy)cyclohexane at 99% used as carbonyl protecting agent in steroid synthesis. Specifically enumerated under HTS 2911.00.10.00 within acetals and hemiacetals subchapter. Essential for selective organic transformations in fine chemical manufacturing.
Isopropoxy-Protected Cyclohexanone Derivative
Laboratory reagent 1,1-bis(1-methylethoxy)cyclohexane serving as protected form of cyclohexanone. Classified under HTS 2911.00.10.00 due to specific acetal structure meeting chapter definition (a). Used in asymmetric synthesis and natural product isolation.