1072-32-8

Usage

Uses

Used in Pesticide Industry:
DODECYL ISOTHIOCYANATE is used as an active ingredient in the production of insecticides and fungicides for its ability to effectively control and eliminate pests, thereby protecting crops and enhancing agricultural productivity.
Used in Pharmaceutical Industry:
DODECYL ISOTHIOCYANATE is used as a building block for the modification of biomolecules in the manufacturing of pharmaceuticals. Its versatile properties allow for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
DODECYL ISOTHIOCYANATE is used as a key component in the development of agrochemicals, contributing to the improvement of crop protection and yield.
Used in Organic Synthesis:
DODECYL ISOTHIOCYANATE is used as a reagent in various chemical reactions, enabling the synthesis of specialty chemicals and the development of new compounds with specific properties and applications.
Used in Chemical Research:
DODECYL ISOTHIOCYANATE is used as a research tool in the study of chemical reactions and the development of new methodologies, further expanding its applications in the scientific community.

InChI:InChI=1/C13H25NS/c1-2-3-4-5-6-7-8-9-10-11-12-14-13-15/h2-12H2,1H3

Upstream product

• 75-15-0 carbon disulfide 
• 124-22-1 n-Dodecylamine 
• 463-71-8 thiophosgene 
• 2926-29-6 Langlois reagent 

Downstream Products

• 2422-90-4 dodecyl-thiourea 
• 31979-30-3 N-(4-ethoxy-phenyl)-N'-dodecyl-thiourea 
• 1047621-21-5 C₄₇H₈₂N₄O₁₀S 
• 1427279-13-7 5-(3-chlorophenyl)-4-dodecyl-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 1427279-08-0 1-(3-chlorobenzoyl)-4-dodecylthiosemicarbazide 
• 1269668-30-5 C₃₀H₄₇N₂PS 
• 135884-64-9 C₂₈H₄₈Cl₂N₄S*BrH 
• 135660-17-2 C₂₀H₃₂Cl₂N₄S 
• 7505-51-3 1,3-didodecylthiourea 
• 1192240-70-2 C₃₁H₄₇N₂PS 

Relevant academic research and scientific papers

Isothiocyanation of amines using the Langlois reagent

The Langlois reagent was found to be effective for the isothiocyanation of primary amines in the presence of copper iodide and diethyl phosphonate.

NOVEL LIPIDS AND NOVEL PHOSPHOLIPIDS STRUCTURES

The invention relates to a lipids comprising or consisting of 1,3-diamidolipids or/and 1,2-diamidolipids or/and 2,3-diamidolipids or/and 1,3-diurealipids or/and 1,2-diurealipids or/and 2,3-diurealipids or/and 1,3 -dithiourealipids or/and 1,2-dithiourealipids or/and 2,3-dithiourealipids or/and 1,3-diacylurealipids or/and 1,2-diacylurealipids or/and 2,3-diacylurealipids or/and 1 -amidolipids or/and 1-urealipids or/and 1-thiourealipids or/and 1-acylurealipids or/and cyclic-amidolipids or/and cyclic urealipids or/and cyclic thiourealipids or/and cyclic acylurealipids, and their medical and non-medical use.

Synthesis and solution thermodynamic study of rigidified and functionalised EGTA derivatives

The synthesis of a new series of EGTA (ethyleneglycol-bis(2- aminoethylether)-N,N,N′,N′-tetraacetic acid) derivatives incorporating aromatic and functionalized aromatic moieties into the oxoethylenic bridge is described. A solution thermodynamic study was

Alkanethioimidoyl Radicals: Evaluation of β-Scission Rates and of Cyclization onto S-Alkenyl Substituents

Thioimidoyl radicals were generated by addition of alkylsulfanyl radicals to alkyl isonitriles and were characterized by electron paramagnetic resonance (EPR) spectroscopy. The β-scissions of their C·S-C bonds were studied by variable-temperature EPR spectroscopy and the fragmentation rate constants and activation energies were calculated. The scission rates depend on the stability of the released alkyl radicals but in any case, at room temperature, the processes were fast. Data collected on similar oxyimidoyls showed that their fragmentations are slightly slower compared to those of analogous thioimidoyls. The scission rates of selenoimidoyls could not be studied by EPR and were evaluated by theoretical calculations. EPR experiments also enabled both β-scission and 5-exo ring closure rate constants of two S-but-3-enyl-substituted imidoyl radicals to be determined, showing that cyclization prevails only at low temperatures. Density functional theory (DFT) theoretical calculations predicted that the fragmentation process preferentially occurs from the s-cis rotamers (X-C bond) of the imidoyl radicals. Thio- and seleno-imidoyls (but not oxyimidoyls) prefer s-trans conformations so that their fragmentations involve prior rotation about the X-C bond.

A general synthesis of isothiocyanates from dithiocarbamates using claycop

A Convenient and simple synthesis of alkyl, aryl and amino acid isothiocyanates is described by the decomposition of ammonium dithiocarbamates using Claycop in mild conditions.