6-Azaindole

Base Information

Chemical Name:6-Azaindole
CAS No.:271-29-4
Molecular Formula:C7H6N2
Molecular Weight:118.138
Hs Code.:29339980
European Community (EC) Number:664-233-5
DSSTox Substance ID:DTXSID20181562
Nikkaji Number:J1.862.984D,J72.956F
Wikidata:Q72444314
Mol file:271-29-4.mol

Synonyms:6-azaindole

Suppliers and Price of 6-Azaindole

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
6-Azaindole
2.5g
$ 50.00

TRC
6-Azaindole
25g
$ 335.00

SynChem
6-Azaindole 95+%
5 g
$ 125.00

SynChem
6-Azaindole 95+%
1 g
$ 40.00

Matrix Scientific
6-Azaindole 96%
1g
$ 17.00

Matrix Scientific
6-Azaindole 96%
5g
$ 54.00

Matrix Scientific
6-Azaindole 96%
10g
$ 88.00

Labseeker
6-Azaindole 98
25g
$ 538.00

Crysdot
1H-Pyrrolo[2,3-c]pyridine 98%
10g
$ 119.00

Chemenu
1H-pyrrolo[2,3-c]pyridine 95%+
25g
$ 214.00

Total 125 raw suppliers

Chemical Property of 6-Azaindole

Chemical Property:

Appearance/Colour:off-white to yellowish crystalline powder
Vapor Pressure:0.003mmHg at 25°C
Melting Point:136-137 °C
Refractive Index:1.697
Boiling Point:295.761 °C at 760 mmHg
PKA:14.66±0.30(Predicted)
Flash Point:137.4 °C
PSA：28.68000
Density:1.242 g/cm³
LogP:1.56290
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
Sensitive.:Air & Light Sensitive
Water Solubility.:Soluble in water (hardly), methanol and chloroform.
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:118.053098200
Heavy Atom Count:9
Complexity:103

Purity/Quality:

99% ^*data from raw suppliers

6-Azaindole ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CNC2=C1C=CN=C2
Uses 6-Azaindole is an indole derivative and useful synthetic intermediate.

Technology Process of 6-Azaindole

There total 16 articles about 6-Azaindole 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: 97.0%