34678-40-5 Usage
Structure
Cyclohexanol derivative with a hexenyl side chain
Appearance
Colorless to pale yellow liquid
Odor
Pleasant, characteristic odor
Taste
Pleasant, characteristic taste
Solubility
Soluble in organic solvents, slightly soluble in water
Boiling point
Approximately 250°C
Density
Approximately 0.9 g/cm3
Fragrance industry
Used to create natural and synthetic scents for perfumes, soaps, and other consumer products
Flavor industry
Used to enhance the taste of various food products
Medicinal applications
Studied for potential biological and pharmacological activities
Natural sources
Found in fruits and flowers
Synthesis
Can be synthesized for use in various industries
Safety
Generally considered safe for use in the fragrance and flavor industries, but potential for skin irritation or sensitization in some individuals
Environmental impact
Biodegradable, but potential for aquatic toxicity depending on concentration and environmental conditions
Regulatory status
Regulated by various organizations, such as the International Fragrance Association (IFRA) and the Flavor and Extract Manufacturers Association (FEMA), to ensure safe use in consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 34678-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34678-40:
(7*3)+(6*4)+(5*6)+(4*7)+(3*8)+(2*4)+(1*0)=135
135 % 10 = 5
So 34678-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O/c1-2-3-4-6-9-12(13)10-7-5-8-11-12/h6,9,13H,2-5,7-8,10-11H2,1H3/b9-6+
34678-40-5Relevant academic research and scientific papers
N-heterocyclic carbene-catalyzed hydrosilylation of styryl and propargylic alcohols with dihydrosilanes
Zhao, Qiwu,Curran, Dennis P.,Malacria, Max,Fensterbank, Louis,Goddard, Jean-Philippe,Lacote, Emmanuel
supporting information; experimental part, p. 9911 - 9914 (2011/10/05)
Reducing alkenes to tears: Addition of structurally diverse N-heterocyclic carbenes (NHCs) to silicon allows the reduction of propargylic and styryl alcohols through an organocatalyzed silylation/direct hydride transfer tandem reaction (see scheme). Catalytic turnover is enabled by the switch to and from hypervalent silicon. This provides a new synthetic application of NHC-main group element complexes. Copyright
NiCl2/CrCl2-mediated coupling reaction of ketones with alkenyl(or alkynyl, aryl) halides accomplished in the presence of a bipyridyl-type ligand
Chen, Chinpiao
, p. 1311 - 1312 (2007/10/03)
In this work, alkenyl halides (or triflates) and alkynyl (or aryl) halides are readily coupled with ketones in tetrahydrofuran in the presence of ligand 1, NiCl2 and CrCl2 at room temperature subsequently yielding the corresponding allylic alcohols, propargylic alcohols and benzylic alcohols.
