2-Methyl-6-nitroindoline

Base Information

Chemical Name:2-Methyl-6-nitroindoline
CAS No.:51134-82-8
Molecular Formula:C9H10N2O2
Molecular Weight:178.19
Hs Code.:2933990090
DSSTox Substance ID:DTXSID60566955
Nikkaji Number:J89.605E
Mol file:51134-82-8.mol

Synonyms:2-Methyl-6-nitroindoline;51134-82-8;2,3-Dihydro-2-methyl-6-nitro-1H-indole;2-methyl-6-nitro-2,3-dihydro-1H-indole;6-nitro-2-methylindoline;DTXSID60566955;AMY38793;AKOS016005624

Suppliers and Price of 2-Methyl-6-nitroindoline

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

Crysdot
2-Methyl-6-nitroindoline 95+%
1g
$ 455.00

Chemenu
2-Methyl-6-nitroindoline 95%
1g
$ 430.00

American Custom Chemicals Corporation
2-METHYL-6-NITROINDOLINE 95.00%
5MG
$ 501.34

Alichem
2-Methyl-6-nitroindoline
1g
$ 401.76

Total 8 raw suppliers

Chemical Property of 2-Methyl-6-nitroindoline

Chemical Property:

Boiling Point:306.9±31.0 °C(Predicted)
PKA:3.45±0.40(Predicted)
PSA：57.85000
Density:1.217±0.06 g/cm3(Predicted)
LogP:2.61250
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:178.074227566
Heavy Atom Count:13
Complexity:214

Purity/Quality:

97% ^*data from raw suppliers

2-Methyl-6-nitroindoline 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC2=C(N1)C=C(C=C2)[N+](=O)[O-]

Technology Process of 2-Methyl-6-nitroindoline

There total 3 articles about 2-Methyl-6-nitroindoline 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: 68.0%

: 6872-06-6
2-methyl indoline

: 51134-82-8
2-methyl-6-nitro-2,3-dihydro-1H-indole

Guidance literature:: With sulfuric acid; nitric acid; at 0 ℃; for 1h;
DOI:10.1016/j.bmc.2008.04.059

Reference yield:

: 95-20-5
2-methyl-1H-indole

: 51134-82-8
2-methyl-6-nitro-2,3-dihydro-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: Na(CN)BH₃, AcOH / Ambient temperature

2: 70percent aq. HNO₃, H₂SO₄ / 0.08 h / 0 °C

With sulfuric acid; nitric acid; sodium cyanoborohydride; acetic acid;
DOI:10.1016/S0960-894X(98)00107-3