4632-01-3 Usage
General Description
2-sec-butyl-cyclohexanol is a chemical compound that belongs to the class of cyclohexanols, which are cyclic alcohols. It has a molecular formula of C10H20O and a molecular weight of 156.27 g/mol. 2-SEC-BUTYL-CYCLOHEXANOL is a colorless liquid with a slightly sweet and floral odor. It is primarily used as a fragrance ingredient in the production of various consumer products such as perfumes, soaps, and cosmetics. Additionally, it is also used as a solvent in the manufacturing of coatings, adhesives, and cleaning agents. 2-sec-butyl-cyclohexanol is considered to have low toxicity and is not expected to cause significant harm to human health or the environment when used as intended.
Check Digit Verification of cas no
The CAS Registry Mumber 4632-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4632-01:
(6*4)+(5*6)+(4*3)+(3*2)+(2*0)+(1*1)=73
73 % 10 = 3
So 4632-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-3-8(2)9-6-4-5-7-10(9)11/h8-11H,3-7H2,1-2H3
4632-01-3Relevant articles and documents
Isomerisations of cycloalkene- and bicycloalkene-derived achiral epoxides by enantioselective α-deprotonation
Hodgson, David M.,Lee, Gary P.,Marriott, Robert E.,Thompson, Alison J.,Wisedale, Richard,Witherington, Jason
, p. 2151 - 2161 (2007/10/03)
Enantioselective α-deprotonation-rearrangement of cis-cyclooctene oxide 1 using organolithiums in the presence of (-)-sparteine 4 or (-)-α-isosparteine 5 gives the (-)-alcohol 2 in good yields and ees. The use of C2-symmetric bisoxazolines (-)-6a-d as ligands allows access to the (+)-alcohol 2. (-)-α-Isosparteine 5 functions as an efficient asymmetric ligand catalyst in the rearrangement of 1. The α-deprotonation process can be extended to other cycloalkene-derived achiral epoxides 7, 9, 11, 15 and 19. Lithium amide-induced transformations of rigid bicycloalkene-derived epoxides (25, 34 and 42) are described, providing insight into the rearrangement mechanisms which operate following α-lithiation in such systems. The enantioselective α-deprotonation-rearrangement of bicycloalkene-derived epoxides (25, 29 and 42) to ketones (28, 33 and 44 respectively) is described.
