Quinoxaline-5-sulfonyl chloride

Base Information

Chemical Name:Quinoxaline-5-sulfonyl chloride
CAS No.:844646-88-4
Molecular Formula:C8H5 Cl N2 O2 S
Molecular Weight:228.659
Hs Code.:2933990090
European Community (EC) Number:897-525-8
DSSTox Substance ID:DTXSID10582120
Wikidata:Q82473443
Mol file:844646-88-4.mol

Synonyms:Quinoxaline-5-sulfonyl chloride;844646-88-4;5-quinoxalinesulfonyl chloride;Quinoxaline-5-sulfonylchloride;5-Quinoxalinesulfonylchloride;8-Quinoxalinesulfonyl chloride;AMY881;SCHEMBL1886785;DTXSID10582120;NAKORIYAIZIQHQ-UHFFFAOYSA-N;MFCD12827951;ZB1466;AKOS006336839;AS-33251;CS-0110639;A840792;J-517945

Suppliers and Price of Quinoxaline-5-sulfonyl chloride

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-QuinoxalinesulfonylChloride
10mg
$ 195.00

Medical Isotopes, Inc.
5-QuinoxalinesulfonylChloride
10 mg
$ 675.00

American Custom Chemicals Corporation
QUINOXALINE-5-SULFONYL CHLORIDE 95.00%
10G
$ 1334.03

American Custom Chemicals Corporation
QUINOXALINE-5-SULFONYL CHLORIDE 95.00%
5G
$ 909.56

AK Scientific
Quinoxaline-5-sulfonylchloride
10g
$ 1357.00

Total 39 raw suppliers

Chemical Property of Quinoxaline-5-sulfonyl chloride

Chemical Property:

PSA：68.30000
LogP:2.63810
XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:227.9760263
Heavy Atom Count:14
Complexity:301

Purity/Quality:

99% ^*data from raw suppliers

5-QuinoxalinesulfonylChloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=NC=CN=C2C(=C1)S(=O)(=O)Cl
Uses Quinoxaline-5-sulfonyl chloride is used in optimization studies relating to the identification of anthranilic sulfonamides and their activity as selective cholecystokinin-2 receptor antagonists. 5-Quinoxalinesulfonyl Chloride is used in optimization studies relating to the identification of anthranilic sulfonamides and their activity as selective cholecystokinin-2 receptor antagonists.

Technology Process of Quinoxaline-5-sulfonyl chloride

There total 3 articles about Quinoxaline-5-sulfonyl chloride 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: 86.0%

: C₈H₆N₂S

: 844646-88-4
quinoxaline-5-sulfonyl chloride

Guidance literature:: C₈H₆N₂S; With formic acid; chlorine; In dichloromethane; water; at 0 ℃; for 0.0833333h;

With sodium hydroxide; In dichloromethane; water;

Reference yield: 73.0%

: 16566-20-4
quinoxalin-5-ylamine

: 844646-88-4
quinoxaline-5-sulfonyl chloride

Guidance literature:: quinoxalin-5-ylamine; With hydrogenchloride; sodium nitrite; In water; at -12 - -5 ℃;

With thionyl chloride; copper dichloride; In water; at 1 ℃;

Reference yield:

: 3694-52-8
2,3-diamino-nitrobenzene

: 844646-88-4
quinoxaline-5-sulfonyl chloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 6 h / Reflux

2.1: hydrogenchloride; zinc / water

3.1: sodium nitrite; hydrogenchloride / water / -12 - -5 °C

3.2: 1 °C

With hydrogenchloride; zinc; sodium nitrite; In ethanol; water; 3.2: |Sandmeyer Reaction;