Urea, (nitrosomethyl)-

Base Information

• Chemical Name: Urea, (nitrosomethyl)-
• CAS No.: 36851-80-6
• Molecular Formula: C2H5N3O2
• Molecular Weight: 103.081
• Hs Code.: 2924199090
• DSSTox Substance ID: DTXSID90190328
• Nikkaji Number: J325.147K
• Wikidata: Q72496241
• Mol file: 36851-80-6.mol

Synonyms:Urea, (nitrosomethyl)-;36851-80-6;Nitrosomethyl urea;(nitrosomethyl)urea;SCHEMBL306978;DTXSID90190328;RHGYANGWZZFRIJ-UHFFFAOYSA-N;AKOS006340971

Chemical Property of Urea, (nitrosomethyl)-

Chemical Property:

• Boiling Point: 188.3°Cat760mmHg
• Flash Point: 67.7°C
• PSA: 85.54000
• Density: 1.58g/cm³
• LogP: 0.28330
• XLogP3: -1.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 103.038176411
• Heavy Atom Count: 7
• Complexity: 81

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Nitrogen Compounds -> Other Nitrogen Compounds
• Canonical SMILES: C(NC(=O)N)N=O

Technology Process of Urea, (nitrosomethyl)-

There total 1 articles about Urea, (nitrosomethyl)- 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:

→ nitrosomethylurea (36851-80-6)

Guidance literature:

Reference yield: 100.0%

nitrosomethylurea (36851-80-6) + phenylacetic acid (103-82-2) → benzeneacetic acid methyl ester (101-41-7)

Guidance literature:

With potassium hydroxide; In diethyl ether; at 0 ℃; Inert atmosphere;

DOI:10.1021/ol101580y

Reference yield: 97.0%

nitrosomethylurea (36851-80-6) + 1,4,5,6-tetrakis(p-tolyl)-7-thiabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid S-oxide → dimethyl 1,4,5,6-tetrakis(p-tolyl)-7-thiabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate S-oxide

Guidance literature:

nitrosomethylurea; With potassium hydroxide; In diethyl ether; water; at 0 ℃;

1,4,5,6-tetrakis(p-tolyl)-7-thiabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid S-oxide; In diethyl ether; water; at 20 ℃; for 5h;

DOI:10.1080/10426507.2015.1100191

Downstream raw materials:

diazomethane

methyl 3-hydroxyquinoline-8-carboxylate

3-(2,6-Dichloro-4-nitro-phenoxy)-quinoline-6-carboxylic acid methyl ester

methyl 5-fluoro-2-methyl-1H-3-indenylacetate