24434-24-0 Usage
Chemical structure
Cyclohexanol derivative
Explanation
Different sources of media describe the Explanation of 24434-24-0 differently. You can refer to the following data:
1. The compound is derived from cyclohexanol, which is a type of alcohol containing a cyclohexane ring with a hydroxyl group attached.
2. The compound contains three functional groups a hydroxyl group (-OH), an ethyl group (-CH2CH3), and a cyclohexyl group (a six-membered ring with two CH2 groups attached).
3. Due to its pleasant smell, 1-[2-(1-hydroxycyclohexyl)ethyl]cyclohexan-1-ol is used in the production of fragrances and perfumes to provide a desirable scent.
4. The compound can be used as a starting material or intermediate in the synthesis of various other organic compounds, making it a versatile building block in chemical reactions.
5. The compound may have potential uses in the development of products in the pharmaceutical and cosmetic industries, although specific applications are not mentioned in the provided material.
6. Due to its various applications in different industries, 1-[2-(1-hydroxycyclohexyl)ethyl]cyclohexan-1-ol is considered a valuable chemical compound with significant industrial and commercial importance.
Functional groups
Hydroxyl group, ethyl group, and cyclohexyl group
Application in fragrances and perfumes
Pleasant odor
Precursor in organic synthesis
Synthesis of other organic compounds
Potential applications
Pharmaceutical and cosmetic industries
Industrial and commercial uses
Valuable chemical compound
Check Digit Verification of cas no
The CAS Registry Mumber 24434-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24434-24:
(7*2)+(6*4)+(5*4)+(4*3)+(3*4)+(2*2)+(1*4)=90
90 % 10 = 0
So 24434-24-0 is a valid CAS Registry Number.
24434-24-0Relevant articles and documents
Baitinger,Schleyer
, p. 989 (1964)
TiCl4/Mg/BrCH2CH2Br Reagent System: A 1,2-Diorganometallic Equivalent
Rao, S. Achyutha,Periasamy, M.
, p. 1583 - 1586 (1988)
1,2-Diorganometallic species generated utilizing the TiCl4/Mg/BrCH2CH2/Br reagent system reacts with ketones to give the corresponding 1,4-diols and/or 1,2-diols in moderate yields.
Synthesis and Applications of Tetrahydrofuran-Stable Substituted (3-Lithioxyalkyl)- and (4-Lithioxyalkyl)lithiums, Modified with Magnesium 2-Ethoxyethoxide
Kostas, Ioannis D.,Screttas, Constantinos G.
, p. 5575 - 5577 (2007/10/03)
Substituted hydroxyalkyl phenyl sulfides 3 have been synthesized from the corresponding allylic or homoallylic alcohols 2. Regiospecific cleavage of the C - SPh bond of the sulfides 3 by lithium dispersion in tetrahydrofuran (THF) led to the synthesis of substituted (3-lithioxyalkyl)- and (4-lithioxyalkyl)lithiums 4, most of which share the ω carbon with a carbocyclic ring. The organolithiums were modified with magnesium 2-ethoxyethoxide in order to suppress their reactivity toward THF cleavage, thus offering the advantage of preparing storable ethereal solutions of certain types of (lithioxyalkyl)lithiums. This strategy appears to be of rather broad scope. The functionalized organolithiums prepared in this way react normally with electrophilic reagents with yields in the range 35-55%. Thus, carboxylations of 4 yielded lactones 5, some of which are natural products, while reactions of 4 with benzophenone and cyclic ketones yielded 1,4- and 1,5-diols 6 and 7, respectively.
