5-Chloro-1-methylindole

Base Information

Chemical Name:5-Chloro-1-methylindole
CAS No.:112398-75-1
Molecular Formula:C9H8ClN
Molecular Weight:165.622
Hs Code.:2933998090
DSSTox Substance ID:DTXSID30445985
Nikkaji Number:J292.134K
Wikidata:Q82264540
Mol file:112398-75-1.mol

Synonyms:5-Chloro-1-methylindole;112398-75-1;5-chloro-1-methyl-1H-indole;1H-Indole, 5-chloro-1-methyl-;5-chloro-1-methyl-indole;1-methyl-5-chloroindole;1-Methyl-5-chloro-1H-indole;SCHEMBL1092569;DTXSID30445985;UAUJZFNYIBXEDG-UHFFFAOYSA-N;MFCD11044848;AKOS006307604;BS-26048;FT-0731853;A802569

Suppliers and Price of 5-Chloro-1-methylindole

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

SynQuest Laboratories
5-Chloro-1-methylindole 95%
1 g
$ 696.00

Crysdot
5-Chloro-1-methyl-1H-indole 97%
1g
$ 391.00

Chemenu
5-Chloro-1-methyl-1H-indole 95%+
1g
$ 369.00

Chemcia Scientific
5-Chloro-1-methyl-1H-indole 95%
5 G
$ 960.00

Apolloscientific
5-Chloro-1-methylindole 95%
1g
$ 435.00

AccelPharmtech
5-chloro-1-methyl-1H-Indole 97.00%
5G
$ 2180.00

Total 11 raw suppliers

Chemical Property of 5-Chloro-1-methylindole

Chemical Property:

Melting Point:35 °C(Solv: cyclohexane (110-82-7))
Boiling Point:278.4±13.0 °C(Predicted)
PSA：4.93000
Density:1.18±0.1 g/cm3(Predicted)
LogP:2.83170
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:165.0345270
Heavy Atom Count:11
Complexity:149

Purity/Quality:

97% ^*data from raw suppliers

5-Chloro-1-methylindole 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C=CC2=C1C=CC(=C2)Cl

Technology Process of 5-Chloro-1-methylindole

There total 18 articles about 5-Chloro-1-methylindole 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: 100.0%

: 17422-32-1
5-chloro-1H-indole

: 74-88-4
methyl iodide

: 112398-75-1
5-chloro-1-methyl-1H-indole

Guidance literature:: 5-chloro-1H-indole; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h; Schlenk technique;

methyl iodide; In tetrahydrofuran; at 20 ℃; Schlenk technique;
DOI:10.1021/acs.orglett.0c00827

Reference yield: 100.0%

: ethyl acetate n-hexane

: 17422-32-1
5-chloro-1H-indole

: 74-88-4
methyl iodide

: 112398-75-1
5-chloro-1-methyl-1H-indole

Guidance literature:: In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; N,N-dimethyl-formamide;

Reference yield: 99.0%

: 17422-32-1
5-chloro-1H-indole

: 616-38-6
carbonic acid dimethyl ester

: 112398-75-1
5-chloro-1-methyl-1H-indole

Guidance literature:: With magnesium oxide; In N,N-dimethyl-formamide; at 170 ℃; for 0.5h; Microwave irradiation; Green chemistry;
DOI:10.1039/c4ra07240e