N-[(4-bromophenyl)carbamothioyl]benzamide

Base Information

• Chemical Name: N-[(4-bromophenyl)carbamothioyl]benzamide
• CAS No.: 19249-89-9
• Molecular Formula: C14H11BrN2OS
• Molecular Weight: 335.224
• DSSTox Substance ID: DTXSID10354001
• Nikkaji Number: J2.018.030G
• Wikidata: Q82131913
• ChEMBL ID: CHEMBL2236348
• Mol file: 19249-89-9.mol

Synonyms:N-[(4-bromophenyl)carbamothioyl]benzamide;19249-89-9;CHEMBL2236348;Benzamide, N-[[(4-bromophenyl)amino]thioxomethyl]-;N-benzoyl-N'-(4-bromophenyl)thiourea;3-BENZOYL-1-(4-BROMOPHENYL)THIOUREA;1-Benzoyl-3-(4-bromophenyl)thiourea;SCHEMBL12012124;DTXSID10354001;BDBM50486919;STK076657;N-para-bromophenyl-N'-benzoylthiourea;AKOS000492647;AT26583;AN-329/40529945;EN300-18216569;SR-01000401700;SR-01000401700-1;Z56812853

Chemical Property of N-[(4-bromophenyl)carbamothioyl]benzamide

Chemical Property:

• PSA: 76.71000
• LogP: 4.22370
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 333.97755
• Heavy Atom Count: 19
• Complexity: 323

Purity/Quality:

99% ^*data from raw suppliers

N-{[(4-bromophenyl)amino]carbonothioyl}benzamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)NC(=S)NC2=CC=C(C=C2)Br

Technology Process of N-[(4-bromophenyl)carbamothioyl]benzamide

There total 7 articles about N-[(4-bromophenyl)carbamothioyl]benzamide 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: 100.0%

Benzoyl isothiocyanate (532-55-8) + 4-bromo-aniline (106-40-1) → 1-benzoyl-3-(4-bromophenyl)thiourea (19249-89-9)

Guidance literature:

In tetrahydrofuran; at 20 ℃; for 1.2h;

Reference yield: 93.0%

ammonium thiocyanate (1147550-11-5) + benzoyl chloride (98-88-4) + 4-bromo-aniline (106-40-1) → 1-benzoyl-3-(4-bromophenyl)thiourea (19249-89-9)

Guidance literature:

ammonium thiocyanate; benzoyl chloride; With tetrabutylammomium bromide; In acetone; Reflux;

4-bromo-aniline; In acetone; for 1.5h; Reflux;

DOI:10.3906/kim-0912-415

Reference yield: 63.0%

→ 1-benzoyl-3-(4-bromophenyl)thiourea (19249-89-9)

Guidance literature:

In acetone; at 20 ℃; for 3.08333h; Reflux;

upstream raw materials:

Benzoyl isothiocyanate

4-bromo-aniline

ammonium thiocyanate

benzoyl chloride

Downstream raw materials:

benzoic acid methyl ester

1-(4-bromophenyl)thiourea

3-(4-bromophenyl)-1,3-thiazolidine-2,4-dione

(4S)-4-(N-benzyloxycarbonyl-2-aminoethyl)-2-[(4-bromophenyl)amino]imidazoline hydrochloride