(10-Methylanthracen-9-yl)methyl carbamimidothioate hydrochloride

Base Information

• Chemical Name: (10-Methylanthracen-9-yl)methyl carbamimidothioate hydrochloride
• CAS No.: 59474-01-0
• Molecular Formula: C₁₇H₁₆N₂S*ClH
• Molecular Weight: 316.854
• ChEMBL ID: CHEMBL1534248
• NSC Number: 146109
• Mol file: 59474-01-0.mol

Synonyms:(10-methyl-9-anthryl)methyl imidothiocarbamate;NSC 146109;NSC-146109;NSC146109;XI 011;XI-011;XI011 cpd

Chemical Property of (10-Methylanthracen-9-yl)methyl carbamimidothioate hydrochloride

Chemical Property:

• Vapor Pressure: 6.93E-10mmHg at 25°C
• Refractive Index: 1.665
• Boiling Point: 493.6°C at 760 mmHg
• Flash Point: 252.3°C
• PSA: 61.18000
• Density: 1.23g/cm³
• LogP: 5.98580
• Storage Temp.: Desiccate at RT
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 316.0800974
• Heavy Atom Count: 21
• Complexity: 333

Purity/Quality:

99% ^*data from raw suppliers

NSC 146109 hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C2C=CC=CC2=C(C3=CC=CC=C13)CSC(=N)N.Cl
• Uses: This molecule inhibits MDMX expression in breast cancer cells through activating p53 resulting in apoptosis in cancer cells.

Technology Process of (10-Methylanthracen-9-yl)methyl carbamimidothioate hydrochloride

There total 1 articles about (10-Methylanthracen-9-yl)methyl carbamimidothioate hydrochloride 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:

→ Nsc 146109 hydrochloride (59474-01-0)

Guidance literature:

entspr. Chloromethylverb., Thioharnstoff;

DOI:10.1021/jo00881a009