128-09-6 | N-Chlorosuccinimide

Packsize	Purity	Availability	Price	Discounted Price
100g	98%	in stock	$13.00	$9.00
500g	98%	in stock	$16.00	$11.00

Description

• Catalog Number: AA43434
• Chemical Name: N-Chlorosuccinimide
• CAS Number: 128-09-6
• Molecular Formula: C4H4ClNO2
• Molecular Weight: 133.5331
• MDL Number: MFCD00005511
• SMILES: ClN1C(=O)CCC1=O
• NSC Number: 8748

Computed Properties

• Complexity: 129
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• XLogP3: -0.2

Literature

• Cu-Mn spinel oxide catalyzed regioselective halogenation of phenols and N-heteroarenes.

  The Journal of organic chemistry 20120706

• ReactNMR and ReactIR as reaction monitoring and mechanistic elucidation tools: the NCS mediated cascade reaction of α-thioamides to α-thio-β-chloroacrylamides.

  The Journal of organic chemistry 20111202

• Titanium-mediated amination of Grignard reagents using primary and secondary amines.

  Angewandte Chemie (International ed. in English) 20110829

• Oxidation of Z α1-antitrypsin by cigarette smoke induces polymerization: a novel mechanism of early-onset emphysema.

  American journal of respiratory cell and molecular biology 20110801

• One-electron reduction of N-chlorinated and N-brominated species is a source of radicals and bromine atom formation.

  Chemical research in toxicology 20110321

• Chloramine-T and N-chlorosuccinimide: novel reagents for diastereoselective oxidation of bisnaphthols.

  Molecular diversity 20101101

• A method for parallel solid-phase synthesis of iodinated analogs of the cannabinoid receptor type I (CB₁) inverse agonist rimonabant.

  Methods in enzymology 20100101

• Enantiocontrolled synthesis of polychlorinated hydrocarbon motifs: a nucleophilic multiple chlorination process revisited.

  The Journal of organic chemistry 20090116

• General and efficient copper-catalyzed amidation of saturated C-H bonds using N-halosuccinimides as the oxidants.

  The Journal of organic chemistry 20080815

• Cleavage of high-molecular-weight kininogen by elastase and tryptase is inhibited by ferritin.

  American journal of physiology. Lung cellular and molecular physiology 20080301

• Application of H-point standard addition method and partial least squares to the simultaneous kinetic-potentiometric determination of hydrazine and phenylhydrazine.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20080201

• A simple crosslinking method, CLAMP, to map the sites of RNA-contacting domains within a protein.

  Methods in molecular biology (Clifton, N.J.) 20080101

• Reactivity of Pd(II) complexes with electrophilic chlorinating reagents: isolation of Pd(IV) products and observation of C-Cl bond-forming reductive elimination.

  Journal of the American Chemical Society 20071212

• Flow injection chemiluminescence analysis of phenolic compounds using the NCS-luminol system.

  Analytical and bioanalytical chemistry 20060301

• Enantioselective chlorination and fluorination of beta-keto phosphonates catalyzed by chiral Lewis acids.

  Chemical communications (Cambridge, England) 20050314

• Flow injection analysis of riboflavin with chemiluminescence detection using a N-halo compounds-luminol system.

  Luminescence : the journal of biological and chemical luminescence 20050101

• Chemical oxidants acidify solitary complex (SC) neurons in the rat.

  Undersea & hyperbaric medicine : journal of the Undersea and Hyperbaric Medical Society, Inc 20040101

• Flow injection determination of isoniazid using N-bromosuccinimide- and N-chlorosuccinimide-luminol chemiluminescence systems.

  Journal of pharmaceutical and biomedical analysis 20030101

• Properties of chemically oxidized kininogens.

  Acta biochimica Polonica 20030101