35356-70-8 | Methyl 2-acetamidoacrylate

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$14.00	$10.00
5g	98%	in stock	$46.00	$33.00
10g	98%	in stock	$64.00	$45.00
20g	98%	in stock	$97.00	$68.00
25g	98%	in stock	$113.00	$80.00

Description

• Catalog Number: AB49289
• Chemical Name: Methyl 2-acetamidoacrylate
• CAS Number: 35356-70-8
• Molecular Formula: C6H9NO3
• Molecular Weight: 143.1406
• MDL Number: MFCD00013394
• SMILES: COC(=O)C(=C)NC(=O)C
• NSC Number: 156878

Computed Properties

• Complexity: 174
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 0.1

Literature

• Enantioselective synthesis of tryptophan derivatives by a tandem Friedel-Crafts conjugate addition/asymmetric protonation reaction.

  Journal of the American Chemical Society 20120321

• Rhodium-catalyzed asymmetric hydrogenation of olefins with PhthalaPhos, a new class of chiral supramolecular ligands.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120127

• Reverse-flow adsorption for process-integrated recycling of homogeneous transition-metal catalysts.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20110627

• Methyl-2-acetamidoacrylate, an ethyl pyruvate analog, decreases sepsis-induced acute kidney injury in mice.

  American journal of physiology. Renal physiology 20081201

• Methyl mercapturate synthesis: an efficient, convenient and simple method.

  Molecules (Basel, Switzerland) 20081001

• Orthogonal synthesis of indolines and isoquinolines via aryne annulation.

  Journal of the American Chemical Society 20080206

• Catalytic ability of a cationic Ru(II) monochloro complex for the asymmetric hydrogenation of dimethyl itaconate and enamides.

  Inorganic chemistry 20060320

• The ethyl pyruvate analogues, diethyl oxaloproprionate, 2-acetamidoacrylate, and methyl-2-acetamidoacrylate, exhibit anti-inflammatory properties in vivo and/or in vitro.

  Biochemical pharmacology 20051125

• Rh-catalyzed asymmetric hydrogenation of prochiral olefins with a dynamic library of chiral TROPOS phosphorus ligands.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20051104

• Asymmetric hydrogenation using chiral Rh complexes immobilised with a new ion-exchange strategy.

  Organic & biomolecular chemistry 20050421

• C2-symmetric diphosphinite ligands derived from carbohydrates. The strong influence of remote stereocenters on asymmetric rhodium-catalyzed hydrogenation.

  The Journal of organic chemistry 20041029

• Aqueous enantioselective hydrogenation of methyl 2-acetamidoacrylate with Rh-MeDuPHOS occluded in PDMS.

  Chemical communications (Cambridge, England) 20020221