3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid

Base Information

Chemical Name:3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid
CAS No.:101413-75-6
Molecular Formula:C₁₇H₁₄N₂O₄S
Molecular Weight:342.375
Hs Code.:
Mol file:101413-75-6.mol

Synonyms:3-[2-(3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-acetylamino]-benzoic acid;

Suppliers and Price of 3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid

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

Total 1 raw suppliers

Chemical Property of 3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid

Chemical Property:

PSA：120.80000
LogP:3.03740

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid

There total 2 articles about 3-(2-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-2-yl)acetamido)benzoic acid 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: 77.0%

: 17057-07-7
3-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-benzoic acid

: 137-07-5
2-amino-benzenethiol

: 101413-75-6
3-Oxo-2,3-dihydro-1,4-benzothiazin-2-yl-acetyl-3-aminobenzoesaeure

Guidance literature:: In ethanol; Heating;

Reference yield:

: 36847-92-4,42537-54-2
3-[[(2Z)-3-carboxy-1-oxo-2-propen-1-yl]amino]benzoic acid

: 101413-75-6
3-Oxo-2,3-dihydro-1,4-benzothiazin-2-yl-acetyl-3-aminobenzoesaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / CH₃CO₂Na, Ac₂O / 0.17 h / 75 °C

2: 77 percent / ethanol / Heating

With sodium acetate; acetic anhydride; In ethanol;