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.

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

Upstream product

• 115-69-5 2-Amino-2-methylpropane-1,3-diol 
• 103962-90-9 7-methyl-7H-benzocarbazole-10-carbaldehyde 
• 1698-16-4 10-bromo-7H-benzo[c]carbazole 
• 32542-45-3 10-bromo-5,6-dihydro-7H-benzocarbazole 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 158918-24-2 10-bromo-5,6-dihydro-7-methyl-7H-benzocarbazole 
• 158918-23-1 10-bromo-7-methyl-7H-benzocarbazole 

Relevant academic research and scientific papers

Synthesis of 2-methyl-2-[[(7-methyl-7H-benzo[c]carbazol-10-yl) [14C]methyl]amino]. 1,3-propanediol mesylate. A potential antitumor agent

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%.

Phenanthro[2,3-6]thiophene derivatives, pharmaceutical compositions and use

The present invention relates to anti tumor compounds of formula (I) or a monomethyl or monoethyl ether thereof (the compound of formula (I) including these ethers may contain no more than 29 carbon atoms in total); ethers, esters thereof; acid addition salts thereof; wherein Ar is a fused tetracyclic aromatic ring system comprised of 5-membered and 6-membered rings and contains at least one heteroatom and 3 aromatic rings and a total of no more than 18 ring atoms, or a substituted derivative thereof; the heteroatom is preferably oxygen, sulfur or nitrogen; when it is nitrogen this is substituted by hydrogen, methyl or ethyl; R1 contains not more than eight carbon atoms and is a group STR1 wherein m is 0 or 1; R5 is hydrogen; R6 and R7 are the same or different and each is hydrogen or C1-5 alkyl optionally substituted by hydroxy; R8 and R9 are the same or different and each is hydrogen or C1-3 alkyl; STR2 is a five or six-membered saturated carbocyclic ring; R10 is hydrogen, methyl or hydroxymethyl; R11, R12 and R13 are the same or different and each is hydrogen or methyl; R14 is hydrogen, methyl, hydroxy, or hydroxymethyl.