Tetra((2H3)methyl)urea

Base Information

Chemical Name:Tetra((2H3)methyl)urea
CAS No.:51219-89-7
Molecular Formula:C5H12N2O
Molecular Weight:128.068
Hs Code.:28459010
European Community (EC) Number:257-062-9
DSSTox Substance ID:DTXSID00199226
Nikkaji Number:J261.662I
Wikidata:Q83072131
Mol file:51219-89-7.mol

Synonyms:Tetra((2H3)methyl)urea;51219-89-7;TETRAMETHYLUREA-D12;1,1,3,3-tetrakis(trideuteriomethyl)urea;EINECS 257-062-9;1,1,3,3-Tetramethylurea-d12;Tetra[(2H3)methyl]urea;Urea, tetra(methyl-d3)-;C5D12N2O;SCHEMBL11725383;HY-I0983S;DTXSID00199226;1,1,3,3-tetra(?H?)methylurea;C5-D12-N2-O;CS-0567874;D99677

Suppliers and Price of Tetra((2H3)methyl)urea

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Medical Isotopes, Inc.
Tetramethyl-d12-urea
0.1 g
$ 845.00

American Custom Chemicals Corporation
TETRAMETHYLUREA-D12 95.00%
5MG
$ 499.54

Total 12 raw suppliers

Chemical Property of Tetra((2H3)methyl)urea

Chemical Property:

Appearance/Colour:clear colorless liquid
Vapor Pressure:1.16mmHg at 25°C
Melting Point:1 °C
Refractive Index:1.445
Boiling Point:175.2 °C at 760 mmHg
Flash Point:53.9 °C
PSA：23.55000
Density:0.946 g/cm³
LogP:0.22960
XLogP3:0.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:128.170283962
Heavy Atom Count:8
Complexity:78.4

Purity/Quality:

98%min ^*data from raw suppliers

Tetramethyl-d12-urea ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 61
Safety Statements: 53-45

MSDS Files:

Useful:

Canonical SMILES:CN(C)C(=O)N(C)C
Isomeric SMILES:[2H]C([2H])([2H])N(C(=O)N(C([2H])([2H])[2H])C([2H])([2H])[2H])C([2H])([2H])[2H]
Uses Tetramethyl-d12-urea (CAS# 51219-89-7) is a useful isotopically labeled research compound.

Technology Process of Tetra((2H3)methyl)urea

There total 56 articles about Tetra((2H3)methyl)urea 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: 98.0%

: 1780-17-2
quinolin-2-ylmethanol

: 5470-96-2
quinoline 2-carbaldehyde

Guidance literature:: With fluorosulfonyl fluoride; potassium carbonate; dimethyl sulfoxide; at 20 ℃; for 12h; chemoselective reaction;
DOI:10.1002/adsc.201900104

Reference yield: 95.0%

: 91-63-4
2-methylquinoline

: 5470-96-2
quinoline 2-carbaldehyde

Guidance literature:: With selenium(IV) oxide; In 1,4-dioxane; Inert atmosphere;
DOI:10.1002/asia.201601497

Reference yield: 93.0%

: 2-(iodomethyl)-quinoline

: 5470-96-2
quinoline 2-carbaldehyde

Guidance literature:: With toluene-4-sulfonic acid; In dimethyl sulfoxide; at 130 ℃; for 16h; under 760.051 Torr; Schlenk technique;
DOI:10.1039/c9ob00490d