Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate

Base Information

• Chemical Name: Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate
• CAS No.: 6664-57-9
• Molecular Formula: C15H11ClN2O6
• Molecular Weight: 350.7106
• DSSTox Substance ID: DTXSID90409861
• Wikidata: Q82215865

Synonyms:6664-57-9;Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate;DTXSID90409861;AKOS024430700;PIPERONYL N-(2-CHLORO-4-NITROPHENYL)CARBAMATE

Chemical Property of Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate

Chemical Property:

• Vapor Pressure: 4.97E-09mmHg at 25°C
• Boiling Point: 470.7°Cat760mmHg
• Flash Point: 238.4°C
• Density: 1.561g/cm³
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 350.0305638
• Heavy Atom Count: 24
• Complexity: 473

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1OC2=C(O1)C=C(C=C2)COC(=O)NC3=C(C=C(C=C3)[N+](=O)[O-])Cl

Technology Process of Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate

There total 2 articles about Benzo[1,3]dioxol-5-ylmethyl N-(2-chloro-4-nitro-phenyl)carbamate 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:

4-(3-nitrophenyl)thiazol-2-ylamine (57493-24-0) → 4-(3-Nitro-phenyl)-2-<α-(N-methyl-anilino)-acetamino>-thiazol (6664-57-9)

Guidance literature:

Multi-step reaction with 2 steps

1: benzene

2: ethanol

In ethanol; benzene;

Reference yield:

2-chloro-N-(4-(3-nitrophenyl)thiazol-2-yl)acetamide (6125-33-3) + N-methylaniline (100-61-8) → 4-(3-Nitro-phenyl)-2-<α-(N-methyl-anilino)-acetamino>-thiazol (6664-57-9)

Guidance literature:

In ethanol;

upstream raw materials:

2-chloro-N-(4-(3-nitrophenyl)thiazol-2-yl)acetamide

N-methylaniline

4-(3-nitrophenyl)thiazol-2-ylamine

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