516-12-1 | N-Iodosuccinimide

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$6.00	$4.00
10g	98%	in stock	$8.00	$5.00
25g	98%	in stock	$9.00	$6.00
100g	98%	in stock	$28.00	$19.00
250g	98%	in stock	$63.00	$44.00
500g	98%	in stock	$95.00	$66.00

Description

• Catalog Number: AB47314
• Chemical Name: N-Iodosuccinimide
• CAS Number: 516-12-1
• Molecular Formula: C4H4INO2
• Molecular Weight: 224.9845
• MDL Number: MFCD00005512
• SMILES: IN1C(=O)CCC1=O

Computed Properties

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

Literature

• A silver-catalyzed spirocyclization of alkynyl silyl enol ethers.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120625

• Achiral counterion control of enantioselectivity in a Brønsted acid-catalyzed iodolactonization.

  Journal of the American Chemical Society 20120411

• Unexpected anomeric selectivity of a 1-C-arylglycal donor in Kdo glycoside synthesis.

  The Journal of organic chemistry 20120106

• Phenylsulfanylation of 3',4'-unsaturated adenosine employing thiophenol-N-iodosuccinimide leads to 4'-phenylsulfanylcordycepin: synthesis of 4'-substituted cordycepins on the basis of substitution of the phenylsulfanyl leaving group.

  The Journal of organic chemistry 20111104

• En route to sugar-alkaloid conjugates.

  Carbohydrate research 20110906

• Reactivity switching and selective activation of C-1 or C-3 in 2,3-unsaturated thioglycosides.

  Carbohydrate research 20110906

• Synthesis and incorporation of a furan-modified adenosine building block for DNA interstrand crosslinking.

  Chemical communications (Cambridge, England) 20110314

• Tandem reaction of propargylic alcohol, sulfonamide, and N-iodosuccinimide: synthesis of N-(2-iodoinden-1-yl)arenesulfonamide.

  Organic letters 20110304

• Synthesis and electrochemical behaviour of beta-halodehydroamino acid derivatives.

  Amino acids 20100701

• Mild arming and derivatization of natural products via an In(OTf)3-catalyzed arene iodination.

  Organic letters 20100507

• Bohlmann-Rahtz cyclodehydration of aminodienones to pyridines using N-iodosuccinimide.

  Molecules (Basel, Switzerland) 20100430

• Synthesis of neutral glycosphingolipids from Zygomycetes.

  Carbohydrate research 20080908

• Concise synthesis of a pentasaccharide related to the anti-leishmanial triterpenoid saponin isolated from Maesa balansae.

  The Journal of organic chemistry 20080905

• Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst.

  Journal of the American Chemical Society 20080326

• Highly beta-selective, N-iodosuccinimide-mediated nucleosidation to bicyclo- and tricyclo-nucleosides.

  Nucleic acids symposium series (2004) 20080101

• Efficient kinetic resolution of racemic amino aldehydes by oxidation with N-iodosuccinimide.

  Angewandte Chemie (International ed. in English) 20080101

• NIS/H2SO4-Silica: a mild and efficient reagent system for the hydrolysis of thioglycosides.

  Carbohydrate research 20061127

• Odorless benzenethiols in synthesis of thioglycosides and its application for glycosylation reactions.

  Bioorganic & medicinal chemistry letters 20061115

• Gold-catalyzed and N-iodosuccinimide-mediated cyclization of gamma-substituted allenamides.

  The Journal of organic chemistry 20061027

• NIS/TFA: a general method for hydrolyzing thioglycosides.

  Carbohydrate research 20060724

• Contrasting reactivity of thioglucoside and selenoglucoside donors towards promoters: implications for glycosylation stereocontrol.

  Carbohydrate research 20060724

• Synthesis of new, potent avermectin-like insecticidal agents.

  Carbohydrate research 20050704

• Synthesis of 2-iodo-2-deoxy septanosides from a D-xylose-based oxepine: intramolecular cyclization in the absence of a glycosyl acceptor.

  Carbohydrate research 20041004

• Glycosidation with a disarmed glycosyl iodide: promotion and scope.

  Organic letters 20031127

• Stereoselective 1,2-cis glycosylation of 2-O-allyl protected thioglycosides.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20020603

• Stereospecific synthesis of 1,2-cis glycosides by allyl-mediated intramolecular aglycon delivery. 2. The use of glycosyl fluorides.

  Organic letters 20010726

• High-efficiency astatination of antibodies using N-iodosuccinimide as the oxidising agent in labelling of N-succinimidyl 3-(trimethylstannyl)benzoate.

  Nuclear medicine and biology 20010101