sulfathiazole-d4

Base Information

• Chemical Name: sulfathiazole-d4
• CAS No.: 1020719-89-4
• Molecular Formula: C₉H₉N₃O₂S₂
• Molecular Weight: 259.29
• Mol file: 1020719-89-4.mol

Synonyms:

Chemical Property of sulfathiazole-d4

Chemical Property:

• Melting Point: 172-174°C
• Storage Temp.: -20°C Freezer
• Solubility.: DMSO (Slightly), Methanol (Slightly, Heated)

Purity/Quality:

95-99% ^*data from raw suppliers

Sulfathiazole-d4 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Uses: The isotopically labelled antibacterial drug Sulfathiazole The isotopically labelled antibacterial drug Sulfathiazole.

Technology Process of sulfathiazole-d4

There total 6 articles about sulfathiazole-d4 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: 37.0%

C11H7(2)H4N3O3S2 → sulfathiazole-d4 (1020719-89-4)

Guidance literature:

With sodium hydroxide; for 0.5h; Heating;

Reference yield:

aniline-d5 (4165-61-1) → sulfathiazole-d4 (1020719-89-4)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium acetate; acetic acid / 0.5 h / 30 °C

2: chlorosulfonic acid / 0.33 h / 60 °C

3: pyridine / 1 h / 30 - 55 °C

4: sodium hydroxide / 0.5 h / Heating

With chlorosulfonic acid; sodium acetate; acetic acid; sodium hydroxide; In pyridine;

Reference yield:

acetanilide-d5 (15826-91-2) → sulfathiazole-d4 (1020719-89-4)

Guidance literature:

Multi-step reaction with 3 steps

1: chlorosulfonic acid / 0.33 h / 60 °C

2: pyridine / 1 h / 30 - 55 °C

3: sodium hydroxide / 0.5 h / Heating

With chlorosulfonic acid; sodium hydroxide; In pyridine;

upstream raw materials:

aniline-d5

acetanilide-d5

p-acetamidobenzenesulfonyl chloride-d₄

benzene-d6

Refernces