89002-68-6 Usage
Main properties
1. Chemical compound
2. Belongs to the imidazole class
3. Molecular structure contains 4,4,5-trimethyl-2-phenyl group attached to an imidazole ring
4. Used in industrial and pharmaceutical applications
5. Building block in synthesis of organic compounds
6. Pharmaceutical intermediate
7. Biological activities
8. Potential use in drug discovery and development
9. Further research and testing needed
Classification
Chemical compound
Molecular structure
Contains 4,4,5-trimethyl-2-phenyl group attached to an imidazole ring
Applications
Industrial and pharmaceutical
Use
Building block in synthesis of organic compounds and pharmaceutical intermediate
Biological activities
Potential use in drug discovery and development
Research
Further research and testing needed to fully understand properties and applications of 4H-Imidazole, 4,4,5-trimethyl-2-phenyl-
Check Digit Verification of cas no
The CAS Registry Mumber 89002-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89002-68:
(7*8)+(6*9)+(5*0)+(4*0)+(3*2)+(2*6)+(1*8)=136
136 % 10 = 6
So 89002-68-6 is a valid CAS Registry Number.
89002-68-6Relevant academic research and scientific papers
Synthesis and Properties of 4H-Imidazoles
Casey, Michael,Moody, Christopher,Rees, Charles W.
, p. 1389 - 1394 (2007/10/02)
The photolysis of 1-vinyltetrazoles to give 1H-imidazoles is extended to the synthesis of isolable nonaromatic 4H-imidazoles when the vinyl group is terminally disubstituted.Thus photolysis of the 2-phenyltetrazole (7a), prepared from isobutyraldehyde, at
Synthesis and Properties of 4H-Imidazoles
Casey, Michael,Moody, Christopher J.,Rees, Charles W.
, p. 1082 - 1083 (2007/10/02)
Photolysis of alkenyltetrazoles (1) provides the first rational route to simple 4H-imidazoles (2); when unsubstituted at C-5 these are highly reactive towards nucleophiles and rearrange rapidly to the aromatic 1H-imidazoles on heating.
