2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate

Base Information

Chemical Name:2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate
CAS No.:63924-64-1
Molecular Formula:C12H15NO4S
Molecular Weight:269.321
Hs Code.:
DSSTox Substance ID:DTXSID60513626
Wikidata:Q82373533

Synonyms:63924-64-1;DTXSID60513626;2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate

Suppliers and Price of 2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:269.07217913
Heavy Atom Count:18
Complexity:402

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC(=O)OCC(=C)C

Technology Process of 2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)carbamate

There total 1 articles about 2-Methylprop-2-en-1-yl (4-methylbenzene-1-sulfonyl)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:

: 4083-64-1
Tosyl isocyanate

: 513-42-8
3-hydroxy-2-methyl-1-propene

: 63924-64-1
2-methylallyl tosylcarbamate

Guidance literature:: In dichloromethane; at 0 - 25 ℃; Inert atmosphere;
DOI:10.1055/s-0034-1378314

Reference yield: 81.0%

: 63924-64-1
2-methylallyl tosylcarbamate

: 4-(bromomethyl)-4-methyl-3-tosyloxazolidin-2-one

Guidance literature:: With dibromamine-T; potassium tert-butylate; In tetrahydrofuran; at 25 ℃; for 4h; regioselective reaction; Inert atmosphere;
DOI:10.1055/s-0034-1378314