Quinoline-6-carboxamide

Base Information

Chemical Name:Quinoline-6-carboxamide
CAS No.:5382-43-4
Molecular Formula:C10H8N2O
Molecular Weight:172.186
Hs Code.:2933499090
European Community (EC) Number:848-940-8
DSSTox Substance ID:DTXSID40453374
Nikkaji Number:J535.837J
Mol file:5382-43-4.mol

Synonyms:Quinoline-6-carboxamide;5382-43-4;6-Quinolinecarboxamide;MFCD01312760;Oprea1_770849;SCHEMBL249349;SCHEMBL24021437;DTXSID40453374;YMNAJWHTELQUJU-UHFFFAOYSA-N;AMY14446;SC5119;AKOS009285881;SB67813;SY024514;TS-02341;CS-0216513;FT-0729773;EN300-49442;A870626;Z362847974

Suppliers and Price of Quinoline-6-carboxamide

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
Quinoline-6-carboxamide
50mg
$ 45.00

Crysdot
Quinoline-6-carboxamide 95+%
10g
$ 330.00

Chemenu
Quinoline-6-carboxamide 95%
10g
$ 311.00

Atlantic Research Chemicals
Quinoline-6-carboxamide 95%
250mgs:
$ 63.62

Apolloscientific
6-Quinolinecarboxamide 95%
1g
$ 160.00

Apolloscientific
6-Quinolinecarboxamide 95%
5g
$ 595.00

American Custom Chemicals Corporation
6-QUINOLINECARBOXAMIDE 95.00%
5MG
$ 502.51

Alichem
Quinoline-6-carboxamide
10g
$ 400.00

AK Scientific
Quinoline-6-carboxamide
5g
$ 323.00

AccelPharmtech
6-Quinolinecarboxamide 97.00%
25G
$ 4320.00

Total 14 raw suppliers

Chemical Property of Quinoline-6-carboxamide

Chemical Property:

PSA：55.98000
LogP:2.03400
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:172.063662883
Heavy Atom Count:13
Complexity:205

Purity/Quality:

99%, ^*data from raw suppliers

Quinoline-6-carboxamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=CC(=C2)C(=O)N)N=C1

Technology Process of Quinoline-6-carboxamide

There total 9 articles about Quinoline-6-carboxamide 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: 98.0%

: 23395-72-4
quinoline-6-carbonitrile

: 5382-43-4
quinoline-6-carboxamide

Guidance literature:: With manganese(IV) oxide; water; In isopropyl alcohol; at 100 ℃; for 0.5h; under 5171.62 Torr;
DOI:10.1021/ol403591c

Reference yield: 88.0%

: 38896-30-9
6-(methoxycarbonyl)quinoline

: 5382-43-4
quinoline-6-carboxamide

Guidance literature:: With ammonia; water; In methanol; at 45 ℃; for 12h;

Reference yield: 85.0%

: 13327-31-6
6-iodoquinoline

: 64-18-6
formic acid

: 5382-43-4
quinoline-6-carboxamide

Guidance literature:: With palladium diacetate; ammonium bicarbonate; dicyclohexyl-carbodiimide; triphenylphosphine; In acetonitrile; at 90 ℃; Inert atmosphere;
DOI:10.1002/ejoc.201701105