116650-26-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-AMINOMETHYL-CYCLOHEXANOL is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties, contributing to advancements in healthcare and agriculture.
Used in Specialty Chemicals Production:
In the specialty chemicals industry, 3-AMINOMETHYL-CYCLOHEXANOL is employed as a building block for the creation of unique and high-value chemical products. Its versatility in chemical reactions enables the production of a wide range of specialty chemicals with specific applications in various industries.
Used in Fragrance and Flavoring Agents Manufacturing:
3-AMINOMETHYL-CYCLOHEXANOL is utilized in the production of fragrance and flavoring agents due to its ability to impart distinct scents and tastes. Its presence in these agents enhances the sensory experience of various consumer products, such as perfumes, cosmetics, and food items.
Safety Considerations:
As a hazardous substance, 3-AMINOMETHYL-CYCLOHEXANOL requires careful handling to minimize potential health and environmental risks. Proper safety measures, including the use of personal protective equipment and adherence to handling and storage guidelines, should be implemented to ensure the safe use of this chemical compound in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 116650-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,5 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116650-26:
(8*1)+(7*1)+(6*6)+(5*6)+(4*5)+(3*0)+(2*2)+(1*6)=111
111 % 10 = 1
So 116650-26-1 is a valid CAS Registry Number.
InChI:InChI=1S/C7H15NO/c8-5-6-2-1-3-7(9)4-6/h6-7,9H,1-5,8H2
116650-26-1Relevant articles and documents
Selective Catalytic Hydrogenation of Arenols by a Well-Defined Complex of Ruthenium and Phosphorus-Nitrogen PN3-Pincer Ligand Containing a Phenanthroline Backbone
Li, Huaifeng,Wang, Yuan,Lai, Zhiping,Huang, Kuo-Wei
, p. 4446 - 4450 (2017/07/24)
Selective catalytic hydrogenation of aromatic compounds is extremely challenging using transition-metal catalysts. Hydrogenation of arenols to substituted tetrahydronaphthols or cyclohexanols has been reported only with heterogeneous catalysts. Herein, we demonstrate the selective hydrogenation of arenols to the corresponding tetrahydronaphthols or cyclohexanols catalyzed by a phenanthroline-based PN3-ruthenium pincer catalyst.
Cycloalkyl-one-containing benzenesulphonamides
-
, (2008/06/13)
Cycloalkanol[1,2-b]indole-sulphonamides of the formula STR1 where appropriate in an isomeric form, and their salts are disclosed. These compounds are useful to inhibit platelet aggregation and to antagonize thromboxane A2.
