2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine

Base Information

Chemical Name:2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine
CAS No.:74375-66-9
Molecular Formula:C₇H₇N₃S
Molecular Weight:165.219
Hs Code.:
DSSTox Substance ID:DTXSID40225371
Wikidata:Q83104328

Synonyms:74375-66-9;BRN 0129043;2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine;(2,1,3-benzothiadiazol-5-ylmethyl)amine;4-27-00-08099 (Beilstein Handbook Reference);2,1,3-benzothiadiazol-5-ylmethanamine;SCHEMBL3275924;DTXSID40225371;AKOS006282318;(2,1,3-benzothiadiazol-5-yl)methanamine;LS-40488;Benzo[c][1,2,5]thiadiazol-5-ylmethanamine;CS-0286130;EN300-1696975;1-(2,1,3-BENZOTHIADIAZOL-5-YL)METHANAMINE;(2,1,3-Benzothiadiazol-5-ylmethyl)amine, AldrichCPR

Suppliers and Price of 2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine

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

American Custom Chemicals Corporation
(2,1,3-BENZOTHIADIAZOL-5-YLMETHYL)AMINE 95.00%
10G
$ 2279.97

American Custom Chemicals Corporation
(2,1,3-BENZOTHIADIAZOL-5-YLMETHYL)AMINE 95.00%
5G
$ 1491.68

American Custom Chemicals Corporation
(2,1,3-BENZOTHIADIAZOL-5-YLMETHYL)AMINE 95.00%
1G
$ 818.61

Total 3 raw suppliers

Chemical Property of 2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine

Chemical Property:

Vapor Pressure:0.00189mmHg at 25°C
Boiling Point:291.9°Cat760mmHg
Flash Point:130.3°C
PSA：80.04000
Density:1.383g/cm³
LogP:1.85030
XLogP3:0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:165.03606841
Heavy Atom Count:11
Complexity:142

Purity/Quality:

99% ^*data from raw suppliers

(2,1,3-BENZOTHIADIAZOL-5-YLMETHYL)AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=NSN=C2C=C1CN

Technology Process of 2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine

There total 2 articles about 2,1,3-Benzothiadiazol-2(S(sup IV))-5-methanamine 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:

: 1-benzo[1,2,5]thiadiazol-5-ylmethyl-1,3,5,7-tetraaza-adamantanium; bromide

: 74375-66-9
2,1,3-benzothiadiazol-5-ylmethanamine

Guidance literature:: With hydrogenchloride; In ethanol;

Reference yield:

: 65858-50-6
5-bromomethyl-benzo[1,2,5]thiadiazole

: 74375-66-9
2,1,3-benzothiadiazol-5-ylmethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: CHCl₃ / Heating

2: HCl / ethanol

With hydrogenchloride; In ethanol; chloroform;

Reference yield:

: 74375-66-9
2,1,3-benzothiadiazol-5-ylmethanamine

: ethyl N-[(3,4-diaminophenyl)methyl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / dichloromethane / 0.25 h / Cooling with ice; Inert atmosphere

1.2: 5 h / 20 °C / Inert atmosphere

2.1: hydrogen / methanol / 16 h / 20 °C

With hydrogen; triethylamine; In methanol; dichloromethane;