N-Acetyl-S-(3-bromophenyl)cysteine

Base Information

• Chemical Name: N-Acetyl-S-(3-bromophenyl)cysteine
• CAS No.: 126189-97-7
• Molecular Formula: C11H12BrNO3S
• Molecular Weight: 318.191
• DSSTox Substance ID: DTXSID60558956
• Nikkaji Number: J313.337K
• Mol file: 126189-97-7.mol

Synonyms:126189-97-7;N-Acetyl-S-(3-bromophenyl)cysteine;DTXSID60558956;AKOS013906676

Chemical Property of N-Acetyl-S-(3-bromophenyl)cysteine

Chemical Property:

• XLogP3: 2.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 316.97213
• Heavy Atom Count: 17
• Complexity: 288

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC(CSC1=CC(=CC=C1)Br)C(=O)O

Technology Process of N-Acetyl-S-(3-bromophenyl)cysteine

There total 1 articles about N-Acetyl-S-(3-bromophenyl)cysteine 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: 48.0%

N-Acetamidoacrylic acid (5429-56-1) + 3-Bromothiophenol (6320-01-0) → S-(3-Bromophenyl)mercapturic acid (126189-97-7)

Guidance literature:

With piperidine; In 1,4-dioxane; for 3h; Heating;

DOI:10.1021/jo00296a034

upstream raw materials:

N-Acetamidoacrylic acid

3-Bromothiophenol