p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate

Base Information

• Chemical Name: p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate
• CAS No.: 22954-15-0
• Molecular Formula: C₁₈H₁₉Br₂NO₂
• Molecular Weight: 441.162
• DSSTox Substance ID: DTXSID80945647
• Nikkaji Number: J50.099B
• Wikidata: Q82923057
• ChEMBL ID: CHEMBL3246936
• Mol file: 22954-15-0.mol

Synonyms:22954-15-0;BRN 3066988;p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate;4-[bis(2-bromoethyl)amino]phenyl 3-methylbenzoate;Phenol, p-(bis(2-bromoethyl)amino)-, m-methylbenzoate;Benzoic acid, m-methyl-, p-(bis(2-bromoethyl)amino)phenyl ester;CHEMBL3246936;DTXSID80945647

Chemical Property of p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate

Chemical Property:

• Vapor Pressure: 5.19E-11mmHg at 25°C
• Boiling Point: 522.4°Cat760mmHg
• Flash Point: 269.7°C
• PSA: 29.54000
• Density: 1.539g/cm³
• LogP: 4.81040
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 440.97620
• Heavy Atom Count: 23
• Complexity: 353

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=CC=C1)C(=O)OC2=CC=C(C=C2)N(CCBr)CCBr

Technology Process of p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate

There total 1 articles about p-(Bis(2-bromoethyl)amino)phenyl m-methylbenzoate 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:

→ 3-Methylbenzoesaeure-4-(N,N-bis-(2-bromethyl)-amino)-phenylester (22954-15-0)

Guidance literature:

3-Methylbenzoylchlorid, 4-(N,N-Bis-(2-bromethyl)-amino)-phenol, Py., Dampfbad;

DOI:10.1021/jm00303a603

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