29548-13-8 Usage
Specific Content
Different sources of media describe the Specific Content of 29548-13-8 differently. You can refer to the following data:
1. Also known as cyclohexylidene(prop-1-en-2-yl)methanol
2. Consists of 11 carbon atoms, 18 hydrogen atoms, and 1 oxygen atom
3. The methylidene group is a carbon-carbon double bond (C=C) attached to the cyclohexane ring.
4. The propenyl group is a three-carbon chain with a carbon-carbon double bond at one end, and the hydroxyl group is an oxygen atom bonded to a hydrogen atom (-OH).
5. Commonly used in perfumes, soaps, and cosmetics due to its pleasant scent.
6. The compound's unique structure and functional groups make it useful as a starting material or intermediate in the synthesis of other organic compounds.
7. The compound's versatility in various applications, such as fragrances and chemical synthesis, makes it valuable in both the chemical and consumer goods industries.
Structure
Cyclohexane ring with a methylidene group attached
Functional Groups
Propenyl group and hydroxyl group
Usage
Fragrance ingredient in consumer products
Synthesis
Building block in chemical reactions
Applications
Chemical and consumer goods industries
Check Digit Verification of cas no
The CAS Registry Mumber 29548-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,4 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29548-13:
(7*2)+(6*9)+(5*5)+(4*4)+(3*8)+(2*1)+(1*3)=138
138 % 10 = 8
So 29548-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-8-3-5-10(6-4-8)9(2)7-11/h10-11H,1-7H2
29548-13-8Relevant articles and documents
Reactions of Some Cyclic Ethers in Superacids
Baig, Mirza Azam,Banthorpe, Derek V.,Carr, Graham,Whittaker, David
, p. 1981 - 1986 (2007/10/02)
The reactions of some epoxides and tetrahydrofuran derivatives in superacidic media have been studied.The tetrahydrofurans decompose only at 0 deg C or above, yielding, in some cases, unsaturated carbocations which react to give carbocyclic products, though many yield only tar.Cyclohexene oxides decompose more readily; unsubstituted, they slowly form an allylic ion; with one carbon at the epoxide link substituted they yield the ketone, and with both carbons substituted they give the ring-contracted aldehyde.Limonene 1,2-oxide behaves in a similar manner, though yielding small amounts of the ring-contracted protonated aldehyde (10).Reaction of geraniol 2,3-oxide is initially similar but the intermediate is intercepted intramolecularly to yield the hydroxy-iridoid ethers, 3,3,6β-trimethyl-cis-perhydrocyclopentafuran and 3,3,6α-trimethyl-cis-perhydrocyclopentafuran.Protonation of cyclohexene oxide or norbornene oxide yields onium salts, stable at -70 deg C, which show the addition to be either unsymmetrical (i.e. edge protonation) or to take place in two different positions.
