37694-43-2 Usage
Uses
Used in Pharmaceutical Industry:
Cyclohexanamine, 3,3-dimethylis used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to participate in a range of chemical reactions, making it a valuable building block for the development of new drugs and medications.
Used in Rubber Chemical Industry:
In the rubber chemical industry, Cyclohexanamine, 3,3-dimethylis utilized as a curing agent and accelerator in the production of rubber products. Its ability to enhance the curing process and improve the overall properties of rubber materials makes it an essential component in this sector.
Used in Agricultural Chemical Industry:
Cyclohexanamine, 3,3-dimethylis employed as an intermediate in the synthesis of various agricultural chemicals, such as pesticides and herbicides. Its involvement in the production of these chemicals contributes to the development of more effective and targeted solutions for crop protection and management.
Used in Chemical Intermediates:
As a chemical intermediate, Cyclohexanamine, 3,3-dimethylplays a crucial role in the manufacturing of other chemicals. Its versatile chemical properties enable it to be used in a wide range of chemical reactions, facilitating the production of various compounds and materials.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 37694-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37694-43:
(7*3)+(6*7)+(5*6)+(4*9)+(3*4)+(2*4)+(1*3)=152
152 % 10 = 2
So 37694-43-2 is a valid CAS Registry Number.
37694-43-2Relevant academic research and scientific papers
CYCLOALKYL-SUBSTITUTED IMIDAZOLE DERIVATIVE
-
, (2013/03/26)
A compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof, wherein A represents a C3 to C12 cycloalkyl group which may be substituted by one to three selected from a fluoro group, a hydroxy group, a C1 to C6 alkyl group, etc; R1, R2, and R3 each independently represent a hydrogen atom, a fluoro group, or a C1 to C6 alkyl group; R4 represents a hydrogen atom or a prodrug group; and Y represents -CH2-CHR5-CH2-NHR6 (wherein R5 represents a hydrogen atom, a C1 to C6 alkyl group, or a C1 to C6 alkoxy group, and R6 represents a hydrogen atom or a prodrug group), or the like exhibits excellent TAFIa inhibitory activity and is useful as a therapeutic drug for myocardial infarction, angina pectoris, acute coronary syndrome, cerebral infarction, deep vein thrombosis, pulmonary embolism, and the like.
Carbon-13 magnetic resonance: hydrogen involvement in γ-anti substituent effects
Forrest, T. P.,Thiel, J.
, p. 2870 - 2875 (2007/10/02)
Chemical shifts have been determined for the carbons in a series of 3,3-dimethylcyclohexyl derivatives, (substituent = H, CH3, NH2, OH, Cl, Br, I).Comparison of the γ-anti substituent effects at carbons 3 and 5 indicates that presence of axial protons on these carbons causes increased shielding by all of the above substituents.The shielding by γ-anti substituents is decreased by the replacement of either the α or γ protons by methyl groups; the extent of the decrease is dependent upon the substituent and upon the position of the hydrogen which is replaced.
