3-tert-butyl-1H-indole

Base Information

Chemical Name:3-tert-butyl-1H-indole
CAS No.:19013-51-5
Molecular Formula:C12H15N
Molecular Weight:173.258
Hs Code.:
European Community (EC) Number:862-934-2
DSSTox Substance ID:DTXSID401304077
Nikkaji Number:J1.750.087B
Mol file:19013-51-5.mol

Synonyms:3-tert-butyl-1H-indole;19013-51-5;3-t-butylindole;3-(tert-butyl)-1H-indole;SCHEMBL799601;XGXRTERXPBWVFW-UHFFFAOYSA-N;DTXSID401304077;3-(1,1-Dimethylethyl)-1H-indole;EN300-181473;Z1262562296

Suppliers and Price of 3-tert-butyl-1H-indole

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 3-tert-butyl-1H-indole

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:173.120449483
Heavy Atom Count:13
Complexity:180

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1=CNC2=CC=CC=C21

Technology Process of 3-tert-butyl-1H-indole

There total 1 articles about 3-tert-butyl-1H-indole 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:

: 75400-67-8
indole-1-carboxylic acid tert-butyl ester

: 120-72-9
indole

: 19013-51-5
3-tert-butyl-1H-indole

Guidance literature:: With silica gel; In dichloromethane; at 50 ℃; for 8h; under 0.2 Torr; Yield given. Yields of byproduct given;
DOI:10.1016/0040-4039(95)02398-4

Reference yield: 85.0%

: 19013-51-5
3-tert-butyl-1H-indole

: 931-59-9
benzenesulfenyl chloride

: 1054598-57-0
3-tert-butyl-2-phenylsulfanyl-1H-indole

Guidance literature:: In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1002/anie.200801336

Reference yield: 14.0%

: 19013-51-5
3-tert-butyl-1H-indole

: ethyl 2-(2-(4-methoxyphenyl)cyclopropyl)-2-oxoacetate

: ethyl (±)-10-(tert-butyl)-9-(4-methoxyphenyl)-8,9-dihydropyrido[1,2-a]indole-6-carboxylate

Guidance literature:: With N-(trifluoromethanesulfonyl)phosphoramidic acid diphenyl ester; In toluene; at 100 ℃; for 2h; Sealed tube; Inert atmosphere;
DOI:10.1021/acs.orglett.1c00470