458783
1,3-Bis(benzyloxycarbonyl)-2-methyl-2-thiopseudourea
95%
Synonym(s):
1,3-Bis(benzyloxycarbonyl)-2-methylisothiourea, 2-Methyl-1,3-di-Z-isothiourea
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About This Item
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Quality Level
Assay
95%
form
solid
mp
60-63 °C (lit.)
functional group
amine
phenyl
thioether
SMILES string
CS\C(NC(=O)OCc1ccccc1)=N/C(=O)OCc2ccccc2
InChI
1S/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)
InChI key
CGAMNSKIHXUDMK-UHFFFAOYSA-N
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Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Journal of medicinal chemistry, 50(9), 2078-2088 (2007-04-11)
The norepinephrine transporter (NET) substrates [123I]-m-iodobenzylguanidine (MIBG) and [11C]-m-hydroxyephedrine (HED) are used as markers of cardiac sympathetic neurons and adrenergic tumors (pheochromocytoma, neuroblastoma). However, their rapid NET transport rates limit their ability to provide accurate measurements of cardiac nerve density.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(23), 6878-6888 (2005-09-15)
Asymmetric total synthesis of batzelladine A (1) and batzelladine D (2) has been achieved. Our synthesis of batzelladines features 1) stereoselective construction of the cyclic guanidine system by means of successive 1,3-dipolar cycloaddition reaction and subsequent cyclization, 2) direct esterification
Application of molecular topology to the search of novel NSAIDs: experimental validation of activity.
Letters in Drug Design & Discovery, 7(6), 438-445 (2010)
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