120097-91-8 Usage
Organic compound
Yes
It is an organic compound, meaning it primarily consists of carbon and hydrogen atoms, along with other elements like nitrogen and oxygen.
Backbone
1,3-propanediol
The central structure of the molecule is a 1,3-propanediol backbone, which is a three-carbon diol with hydroxyl groups at the first and third carbon atoms.
Substituent
Benzocarbazole group
The 1,3-propanediol backbone is substituted with a benzocarbazole group, which is a fused-ring system consisting of a benzene ring and a carbazole ring.
Industrial and commercial applications
Precursor in polymer, plastic, and pharmaceutical production
The compound is used as a starting material for the synthesis of various polymers, plastics, and pharmaceuticals.
Solvent
Yes
It can act as a solvent in chemical reactions, helping to dissolve other substances and facilitate reactions.
Reagent
Organic synthesis
The compound is used as a reagent in organic synthesis, which involves the formation of new chemical bonds and the synthesis of new organic compounds.
Potential uses
Materials science, organic chemistry, and pharmaceutical research
The compound has potential applications in various fields, including the development of new materials, the study of organic chemistry, and the research and development of pharmaceuticals.
Structure
2-methyl-2-(((7-methyl-7H-benzo(c)carbazol-10-yl)methyl)amino)-
This part of the name describes the specific functional groups and connectivity within the molecule, indicating the presence of a methyl group, an amino group, and a substituted benzocarbazole group.
Check Digit Verification of cas no
The CAS Registry Mumber 120097-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,9 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120097-91:
(8*1)+(7*2)+(6*0)+(5*0)+(4*9)+(3*7)+(2*9)+(1*1)=98
98 % 10 = 8
So 120097-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H24N2O2/c1-22(13-25,14-26)23-12-15-7-9-19-18(11-15)21-17-6-4-3-5-16(17)8-10-20(21)24(19)2/h3-11,23,25-26H,12-14H2,1-2H3
120097-91-8Relevant articles and documents
Synthesis of 2-methyl-2-[[(7-methyl-7H-benzo[c]carbazol-10-yl) [14C]methyl]amino]. 1,3-propanediol mesylate. A potential antitumor agent
Hill,Eaddy
, p. 697 - 706 (1994)
2-Methyl-2-[[(7-methyl-7H-benzo[c]carbazol-yl)methyl]amino]-l,3-propanediol (1, 7U85) was synthesized as the mesylate salt in the [14C]-labelled form with specific activity 48.4 mCi/mmol suitable for metabolism and tissue distribution studies in animals. The synthetic sequence involved the regiospecific synthesis of a bromobenzo[c]carbazole by a modified Fischer indole synthesis, formylation by a Bouveault reaction, and reductive amination. The radiochemical purity was >97.3%.
