1H-Indazole, 3-methyl-1-phenyl-

Base Information

Chemical Name:1H-Indazole, 3-methyl-1-phenyl-
CAS No.:1575-29-7
Molecular Formula:C14H12N2
Molecular Weight:208.263
Hs Code.:
European Community (EC) Number:867-182-9
DSSTox Substance ID:DTXSID00463712
Nikkaji Number:J1.808.441D
Wikidata:Q82288720
Mol file:1575-29-7.mol

Synonyms:3-Methyl-1-phenyl-1H-indazole;1575-29-7;1H-Indazole, 3-methyl-1-phenyl-;1h-indazole,3-methyl-1-phenyl-;3-methyl-1-phenyl-indazole;SCHEMBL10315082;DTXSID00463712;EN300-11688852

Suppliers and Price of 1H-Indazole, 3-methyl-1-phenyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 1H-Indazole, 3-methyl-1-phenyl-

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:208.100048391
Heavy Atom Count:16
Complexity:235

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NN(C2=CC=CC=C12)C3=CC=CC=C3

Technology Process of 1H-Indazole, 3-methyl-1-phenyl-

There total 23 articles about 1H-Indazole, 3-methyl-1-phenyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 2142-69-0
2-bromophenyl methyl ketone

: 532-96-7
N-benzoyl-N'-phenylhydrazine

: 1575-29-7
1-phenyl-3-methyl-1H-indazole

Guidance literature:: 2-bromophenyl methyl ketone; N-benzoyl-N'-phenylhydrazine; With copper(l) iodide; potassium carbonate; 4-hydroxyproline; In 1,4-dioxane; at 60 ℃; for 30h; Inert atmosphere;

With acetic acid; In 1,4-dioxane; at 60 ℃; for 8h; regioselective reaction;
DOI:10.1021/ol300847v

Reference yield: 90.0%

: 1011736-72-3
N-[1-(2-Bromo-phenyl)-eth-(Z)-ylidene]-N'-phenyl-hydrazine

: 1575-29-7
1-phenyl-3-methyl-1H-indazole

Guidance literature:: With copper; sodium t-butanolate; at 110 ℃; for 20h; Inert atmosphere;
DOI:10.1080/00397911.2011.614714

Reference yield: 89.0%

: 209412-48-6
1-(2-anilinophenyl)ethan-1-one oxime

: 1575-29-7
1-phenyl-3-methyl-1H-indazole

Guidance literature:: With bis(trichloromethyl) carbonate; triethylamine; In dichloromethane; at -5 ℃; for 3h; Temperature; chemoselective reaction;
DOI:10.1016/j.tet.2020.130945