5-Bromo-3,3-dimethylindoline

Base Information

Chemical Name:5-Bromo-3,3-dimethylindoline
CAS No.:53388-86-6
Molecular Formula:C10H12BrN
Molecular Weight:226.116
Hs Code.:2933990090
European Community (EC) Number:854-391-5
DSSTox Substance ID:DTXSID10457985
Wikidata:Q82281095
ChEMBL ID:CHEMBL4941294
Mol file:53388-86-6.mol

Synonyms:5-BROMO-3,3-DIMETHYLINDOLINE;53388-86-6;5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole;5-bromo-3,3-dimethyl-1,2-dihydroindole;MFCD16313849;SCHEMBL2343653;5-bromo-3,3-dimethyl-indoline;CHEMBL4941294;DTXSID10457985;CPLGFHHNPVKTBM-UHFFFAOYSA-N;AKOS017411933;SB64262;NS-02837;CS-0054222;EN300-79340;A829555

Suppliers and Price of 5-Bromo-3,3-dimethylindoline

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

TRC
5-Bromo-3,3-dimethylindoline
50mg
$ 285.00

TRC
5-Bromo-3,3-dimethylindoline
10mg
$ 65.00

Crysdot
5-Bromo-3,3-dimethylindoline 95+%
1g
$ 698.00

Chemenu
5-bromo-3,3-dimethylindoline 95%
1g
$ 660.00

Alichem
5-Bromo-3,3-dimethylindoline
1g
$ 1036.68

Alichem
5-Bromo-3,3-dimethylindoline
250mg
$ 391.00

AK Scientific
5-Bromo-3,3-dimethylindoline
250mg
$ 635.00

AK Scientific
5-Bromo-3,3-dimethylindoline
100mg
$ 572.00

Total 10 raw suppliers

Chemical Property of 5-Bromo-3,3-dimethylindoline

Chemical Property:

PSA：12.03000
LogP:3.29020
Storage Temp.:2-8°C(protect from light)
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:225.01531
Heavy Atom Count:12
Complexity:179

Purity/Quality:

99%, ^*data from raw suppliers

5-Bromo-3,3-dimethylindoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(CNC2=C1C=C(C=C2)Br)C

Technology Process of 5-Bromo-3,3-dimethylindoline

There total 12 articles about 5-Bromo-3,3-dimethylindoline 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: 87.0%

: 120902-45-6
5-bromo-3,3-dimethyl-1,3-dihydro-2H-indol-2-one

: 53388-86-6
5-bromo-3,3-dimethylindoline

Guidance literature:: With trimethylamine-N-oxide; In tetrahydrofuran; methanol;

Reference yield: 54.0%

: 78-84-2
isobutyraldehyde

: 589-21-9
(4-bromophenyl)hydrazine

: 53388-86-6
5-bromo-3,3-dimethylindoline

Guidance literature:: (4-bromophenyl)hydrazine; With trifluoroacetic acid; In toluene; acetonitrile; at 20 - 35 ℃;

isobutyraldehyde; In toluene; acetonitrile; at 20 - 35 ℃; for 6h;

With sodium tetrahydroborate; In methanol; toluene; acetonitrile; at -10 - 0 ℃; for 1.5h;