1202497-71-9

Basic information

• Product Name: benzyl N‐(3‐sulfanylpropyl)carbamate
• Synonyms: benzyl N‐(3‐sulfanylpropyl)carbamate
• CAS NO: 1202497-71-9
• Molecular Weight: 225.312
• Mol File: 1202497-71-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: benzyl N‐(3‐sulfanylpropyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl N‐(3‐sulfanylpropyl)carbamate(1202497-71-9)
• EPA Substance Registry System: benzyl N‐(3‐sulfanylpropyl)carbamate(1202497-71-9)

Safety Data

• Hazardous Substances Data: 1202497-71-9(Hazardous Substances Data)

Upstream product

• 53602-19-0 1-[(benzyloxycarbonyl)amino]-3-chloropropane 
• 84792-78-9 1-[(benzyloxycarbonyl)amino]-3-iodopropane 
• 501-53-1 benzyl chloroformate 
• 5041-33-8 N-(Benzyloxycarbonyl)allylamine 
• 1202497-70-8 benzyl N‐[3‐(acetylsulfanyl)propyl]carbamate 

Downstream Products

• 1202497-73-1 C₂₂H₂₈N₂O₄S₂ 
• 1624284-84-9 3-[(3-benzyloxycarbonylamino)propylthio]propyl (methyl 2,4-di-O-acetyl-3-O-benzyl-β-L-idopyranosyluronate)-(1→4)-O-6-O-acetyl-2-azido-3-benzyl-2-deoxy-α-D-glucopyranoside 
• 1624284-85-0 3-[(3-benzyloxycarbonylamino)propylthio]propyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 
• 1624284-86-1 3-[(3-benzyloxycarbonylamino)propylthio]propyl 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 1624284-87-2 3-[(3-benzyloxycarbonylamino)propylthio]propyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 1624284-88-3 3-[(3-benzyloxycarbonylamino)propylthio]propyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside 
• 1624284-89-4 3-[(3-benzyloxycarbonylamino)propylthio]propyl (methyl 2,3-di-O-benzyl-4-O-(4-methoxybenzyl)-β-D-glucopyranosyluronate)-(1-4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 1624284-90-7 3-[(3-benzyloxycarbonylamino)propylthio]propyl (methyl 2-O-acetyl-3-O-benzyl-4-O-(4-methoxybenzyl)-β-L-idopyranosyluronate)-(1→4)-O-6-O-acetyl-2-azido-3-benzyl-2-deoxy-α-D-glucopyranoside 
• 1624284-91-8 3-[(3-benzyloxycarbonylamino)propylthio]propyl (methyl 2,3-di-O-benzyl-4-O-(4-methoxybenzyl)-β-D-glucopyranosyluronate)-(1→4)-O-(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-)-(1→4)-O-(methyl 2,3-di-O-benzyl-β-D-glucopyranosyluronate)-(1→4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 1624284-92-9 3-[(3-benzyloxycarbonylamino)propylthio]propyl (methyl 2-O-acetyl-3-O-benzyl-4-O-(4-methoxybenzyl)-α-L-idopyranosyluronate)-((1→4)-O-6-O-acetyl-2-azido-3-benzyl-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(methyl 2-O-acetyl-3-O-benzyl-α-L-idopyranosyluronate)-(1→4)-O-6-O-acetyl-2-azido-3-benzyl-2-deoxy-α-D-glucopyranoside 
• 3687-18-1 Homotaurin 
• 77693-74-4 3-{[(phenylmethoxy)carbonyl]amino}propane-1-sulfonic acid 

Relevant articles and documents

Substituted ring-type Isothiazole compounds, non-aqueous solution electrolyte agent comprising thereof and lithium secondary battery comprising the same

The present invention relates to a substituted cyclic isothiazole compound, a non-aqueous electrolyte additive containing the same, and a lithium secondary battery comprising the same. The substituted cyclic isothiazole compound of the present invention,

Repairing the thiol-ene coupling reaction

Thiol-ene coupling (TEC) reactions emerged as one of the most useful processes for coupling different molecular units under reaction mild conditions. However, TEC reactions involving weak C-H bonds (allylic and benzylic fragments) are difficult to run and often low yielding. Mechanistic studies demonstrate that hydrogen-atom transfer processes at allylic and benzylic positions are responsible for the lack of efficiency of the radical-chain process. These competing reactions cannot be prevented, but reported herein is a method to repair the chain process by running the reaction in the presence of triethylborane and catechol. Under these reaction conditions, a unique repair mechanism leads to an efficient chain reaction, which is demonstrated with a broad range of anomeric O-allyl sugar derivatives including mono-, di-, and tetrasaccharides bearing various functionalities and protecting groups. In good repair: Undesired hydrogen-atom transfers are responsible for the lack of efficiency in thiol-ene coupling reactions involving allyl glycosides. This competing reaction cannot be prevented but can be very efficiently repaired by carrying out the reaction in the presence of triethylborane and catechol.

SULFOXIMINAMIDE COMPOUNDS FOR COMBATING ANIMAL PESTS

The invention relates to sulfoximinamid compounds of formula (I), to the enantiomers, diastereomers and salts thereof and to compositions comprising such compounds. The invention also relates to the use of the sulfoximinamid compounds, of their salts or o