92155-16-3 Usage
Explanation
1-hexylcyclohexanecarboxylic acid has a total of 14 carbon atoms, 26 hydrogen atoms, and 2 oxygen atoms in its molecular structure.
Explanation
1-HCHCA contains a carboxyl functional group (-COOH) attached to a hexyl chain and a cyclohexane ring, classifying it as a carboxylic acid.
Explanation
The molecular structure of 1-hexylcyclohexanecarboxylic acid consists of a six-carbon hexyl chain connected to a cyclohexane ring.
Explanation
1-HCHCA is a colorless liquid, which means it does not have any color and flows like a liquid at room temperature.
Explanation
1-hexylcyclohexanecarboxylic acid has a very subtle and mild odor, which is not overpowering.
Explanation
1-HCHCA is used in the food industry as a flavoring agent, in the cosmetic industry as a fragrance ingredient, and in the production of pharmaceuticals, surfactants, and other specialty chemicals.
Explanation
1-hexylcyclohexanecarboxylic acid is considered to be safe for use as it is non-toxic and does not cause skin irritation.
Explanation
1-HCHCA is commonly used as a starting material or precursor in various organic synthesis processes and is commercially available for different industrial applications.
Type of compound
Carboxylic acid
Structure
Hexyl chain attached to a cyclohexane ring
Physical state
Colorless liquid
Odor
Faint
Usage
Flavoring agent, fragrance ingredient, and chemical production
Safety
Non-toxic and non-irritating to the skin
Commercial availability
Preccursor in organic synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 92155-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92155-16:
(7*9)+(6*2)+(5*1)+(4*5)+(3*5)+(2*1)+(1*6)=123
123 % 10 = 3
So 92155-16-3 is a valid CAS Registry Number.
92155-16-3Relevant articles and documents
Decarboxylative fluorination of aliphatic carboxylic acids via photoredox catalysis
Ventre, Sandrine,Petronijevic, Filip R.,Macmillan, David W. C.
supporting information, p. 5654 - 5657 (2015/05/20)
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been achieved via visible light-promoted photoredox catalysis. This operationally simple, redox-neutral fluorination method is amenable to a wide variety of carboxylic acids. Photon-induced oxidation of carboxylates leads to the formation of carboxyl radicals, which upon rapid CO2-extrusion and F? transfer from a fluorinating reagent yield the desired fluoroalkanes with high efficiency. Experimental evidence indicates that an oxidative quenching pathway is operable in this broadly applicable fluorination protocol.
