2-Morpholinobenzo[D]thiazol-6-amine

Base Information

Chemical Name:2-Morpholinobenzo[D]thiazol-6-amine
CAS No.:850021-27-1
Molecular Formula:C₁₁H₁₃N₃OS
Molecular Weight:235.31
Hs Code.:
DSSTox Substance ID:DTXSID80368978
Wikidata:Q82155906
ChEMBL ID:CHEMBL1582891
Mol file:850021-27-1.mol

Synonyms:850021-27-1;2-MORPHOLINOBENZO[D]THIAZOL-6-AMINE;2-morpholin-4-yl-1,3-benzothiazol-6-amine;2-(morpholin-4-yl)-1,3-benzothiazol-6-amine;HMS2685H06;MLS001006284;CHEMBL1582891;SCHEMBL14824499;DTXSID80368978;HMS1729H10;MFCD06385031;AKOS001089409;WAY-644841;BS-14046;SMR000384281;CS-0213033;EN300-12219;SR-01000064330;SR-01000064330-1;Z57160355

Suppliers and Price of 2-Morpholinobenzo[D]thiazol-6-amine

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

Matrix Scientific
2-Morpholinobenzo[d]thiazol-6-amine 97%
10g
$ 4050.00

Matrix Scientific
2-Morpholinobenzo[d]thiazol-6-amine 97%
5g
$ 2512.00

Crysdot
2-morpholinobenzo[d]thiazol-6-amine 95+%
1g
$ 564.00

Chemenu
2-morpholinobenzo[d]thiazol-6-amine 95%
1g
$ 533.00

Alichem
2-(Morpholin-4-yl)-1,3-benzothiazol-6-amine
1g
$ 746.28

AK Scientific
2-Morpholin-4-yl-1,3-benzothiazol-6-amine
5g
$ 3441.00

Total 6 raw suppliers

Chemical Property of 2-Morpholinobenzo[D]thiazol-6-amine

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:235.07793322
Heavy Atom Count:16
Complexity:247

Purity/Quality:

97% ^*data from raw suppliers

2-Morpholinobenzo[d]thiazol-6-amine 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1COCCN1C2=NC3=C(S2)C=C(C=C3)N

Technology Process of 2-Morpholinobenzo[D]thiazol-6-amine

There total 5 articles about 2-Morpholinobenzo[D]thiazol-6-amine 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%

: 423738-98-1
2-morpholin-4-yl-6-nitro-1,3-benzothiazole

: 850021-27-1
2-morpholinobenzo[d]thiazol-6-amine

Guidance literature:: With acetic acid; zinc; In ethanol; for 0.5h; Reflux;
DOI:10.1016/j.bmcl.2012.07.022

Reference yield: 82.0%

: 110-91-8,99108-56-2
morpholine

: 2406-90-8
2-chlorobenzothiazol-6-ylamine

: 850021-27-1
2-morpholinobenzo[d]thiazol-6-amine

Guidance literature:: at 180 ℃; for 0.166667h; Microwave irradiation;

Reference yield:

: 6285-57-0
2-amino-6-nitrobenzothiazole

: 850021-27-1
2-morpholinobenzo[d]thiazol-6-amine

Guidance literature:: Multi-step reaction with 3 steps

1: phosphoric acid; copper(II) sulfate; sodium chloride; sodium nitrite

2: triethylamine / dichloromethane

3: acetic acid; zinc / ethanol / 0.5 h / Reflux

With phosphoric acid; copper(II) sulfate; acetic acid; triethylamine; sodium chloride; zinc; sodium nitrite; In ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2012.07.022