2-(4-Chlorophenyl)-1-hydrazinecarbothioamide

Base Information

• Chemical Name: 2-(4-Chlorophenyl)-1-hydrazinecarbothioamide
• CAS No.: 7382-41-4
• Molecular Formula: C7H8ClN3S
• Molecular Weight: 201.68
• Hs Code.: 2930909090
• NSC Number: 379291
• DSSTox Substance ID: DTXSID40377081
• Mol file: 7382-41-4.mol

Synonyms:7382-41-4;2-(4-chlorophenyl)-1-hydrazinecarbothioamide;2-(4-chlorophenyl)hydrazinecarbothioamide;(4-chloroanilino)thiourea;[(4-chlorophenyl)amino]thiourea;2-(4-Chlorophenyl)hydrazine-1-carbothioamide;NSC379291;4-chlorophenylthiosemicarbazide;SCHEMBL7043304;DTXSID40377081;XJVVZHDEYSKSHF-UHFFFAOYSA-N;1-(4-chlorophenyl)thiosemicarbazide;MFCD00456275;STK062306;AKOS005070127;NSC 379291;NSC-379291;SB86568;CS-0306683;FT-0680212;2P-048;EN300-692984;J-505955

Chemical Property of 2-(4-Chlorophenyl)-1-hydrazinecarbothioamide

Chemical Property:

• Vapor Pressure: 0.000365mmHg at 25°C
• Melting Point: 190-200oC
• Boiling Point: 318.3°Cat760mmHg
• Flash Point: 146.3°C
• PSA: 82.17000
• Density: 1.458g/cm³
• LogP: 2.66430
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 201.0127461
• Heavy Atom Count: 12
• Complexity: 157

Purity/Quality:

98%min ^*data from raw suppliers

2-(4-Chlorophenyl)-1-hydrazinecarbothioamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC(=CC=C1NNC(=S)N)Cl

Technology Process of 2-(4-Chlorophenyl)-1-hydrazinecarbothioamide

There total 7 articles about 2-(4-Chlorophenyl)-1-hydrazinecarbothioamide 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: 75.0%

carbon disulfide (75-15-0,12122-00-8) + 4-chloro-aniline (106-47-8) → p-chlorophenyl thiosemicarbazide (7382-41-4)

Guidance literature:

With ammonium hydroxide; hydrazine hydrate; chloroacetic acid; sodium hydroxide; In ethanol; Heating;

DOI:10.1016/j.molstruc.2014.10.024

Reference yield: 43.0%

C7H5ClNS2(1-)*K(1+) → p-chlorophenyl thiosemicarbazide (7382-41-4)

Guidance literature:

With hydrazine hydrate; In ethanol; for 6h; Reflux;

DOI:10.1039/c3ob41109e

Reference yield:

4-chloro-aniline (106-47-8) → p-chlorophenyl thiosemicarbazide (7382-41-4)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / 2 h / 20 °C

2: hydrazine hydrate / ethanol / 6 h / Reflux

With hydrazine hydrate; potassium hydroxide; In ethanol;

DOI:10.1039/c3ob41109e

upstream raw materials:

(Z)-(4-chloro-phenyl)-diazenecarbonitrile

ammonium thiocyanate

N-4-chlorophenylhydrazine

4-chloro-aniline

Downstream raw materials:

2-[N'-(4-chloro-phenyl)-hydrazino]-5-phenyl-thiazol-4-ylamine

thiazolidin-2-one (4-chloro-phenyl)-hydrazone

1-(4-Chloro-phenyl)-5-pyridin-4-yl-1,2-dihydro-[1,2,4]triazole-3-thione

1-(4-Chloro-phenyl)-5-thiophen-2-yl-1,2-dihydro-[1,2,4]triazole-3-thione

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