1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA - Names and Identifiers
Name | dibenzyl [(methylsulfanyl)methylylidene]biscarbamate
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Synonyms | 2-Methyl-1,3-di-Z-isothiourea 1,3-Di-Cbz-2-Methylisothiourea 1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-ISOTHIOUREA 1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA dibenzyl [(methylsulfanyl)methylylidene]biscarbamate 1,3-Bis(benzyloxycarbonyl)-2-methylisothiourea, 2-Methyl-1,3-di-Z-isothiourea Carbamic acid, N-[(methylthio)[[(phenylmethoxy)carbonyl]amino]methylene]-, phenylmethyl ester
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CAS | 25508-20-7
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InChI | InChI=1/C18H18N2O4S/c1-25-16(19-17(21)23-12-14-8-4-2-5-9-14)20-18(22)24-13-15-10-6-3-7-11-15/h2-11H,12-13H2,1H3,(H,19,20,21,22) |
1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA - Physico-chemical Properties
Molecular Formula | C18H18N2O4S
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Molar Mass | 358.41 |
Density | 1.21±0.1 g/cm3(Predicted) |
Melting Point | 60-63°C(lit.) |
Solubility | Chloroform (Slightly), Methanol (Slightly) |
Appearance | Solid |
Color | White to Off-White |
BRN | 9211307 |
pKa | 6.51±0.46(Predicted) |
Storage Condition | -20°C Freezer |
Refractive Index | 1.581 |
1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA - Risk and Safety
Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
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WGK Germany | 3 |
1,3-BIS(BENZYLOXYCARBONYL)-2-METHYL-2-THIOPSEUDOUREA - Introduction
dibenzyl [(methylsulfanyl) methyllylidene] biscarbamate is an organic compound with the chemical formula C15H16N2O4S. The following is a description of its nature, use, preparation and safety information:
Nature:
dibenzyl [(methylsulfonyl) methyllylidene] biscarbamate is a solid powder, colorless or slightly yellow. Its melting point is about 106-109 degrees Celsius. This compound has a unique chemical structure, containing carbonyl and isothiourea functional groups, with strong activity.
Use:
dibenzyl [(methylsulfonyl) methyllylidene] biscarbamate is commonly used as a reagent in organic synthesis. It can be used in the synthesis of other organic compounds and drugs, such as anticancer drugs and antiviral drugs.
Method:
The preparation method of dibenzyl [(methylsulfonyl) methyllylidene] biscarbamate is relatively complicated and requires a series of chemical reactions. A common method is to start with benzyl alcohol and convert it to dibenzyl [(methylsulfanyl) methyllylidene] biscarbamate by chemical reaction.
Safety Information:
Last Update:2024-04-09 02:00:44