626-35-7 | Ethyl nitroacetate

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$8.00	$5.00
10g	97%	in stock	$9.00	$6.00
25g	97%	in stock	$20.00	$14.00
100g	97%	in stock	$49.00	$34.00
250g	97%	in stock	$118.00	$82.00
500g	97%	in stock	$230.00	$161.00

Description

• Catalog Number: AB46126
• Chemical Name: Ethyl nitroacetate
• CAS Number: 626-35-7
• Molecular Formula: C4H7NO4
• Molecular Weight: 133.1027
• MDL Number: MFCD00007403
• SMILES: CCOC(=O)CN(=O)=O
• NSC Number: 42302

Computed Properties

• Complexity: 116
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• XLogP3: 0.5

Literature

• Formation of γ-oxoacids and 1H-pyrrol-2(5H)-ones from α,β-unsaturated ketones and ethyl nitroacetate.

  The Journal of organic chemistry 20101105

• Michael additions versus cycloaddition condensations with ethyl nitroacetate and electron-deficient olefins.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090810

• Ethyl 1-O-tert-butyl-dimethyl-silyl-2,3-O-isopropyl-idene-5-[(2'S)-tetra-hydro-pyran-2-yl-oxy]-d-glycero-α-d-manno-hepto-furonate.

  Acta crystallographica. Section E, Structure reports online 20080801

• Cyclochiral conformers of resorcin[4]arenes stabilized by hydrogen bonds.

  Organic & biomolecular chemistry 20070507

• Functionalization of pyrimidine and purine nucleosides at C4 and C6: C-nucleophilic substitution of their C4- and C6-(1,2,4-triazol-1-yl) derivatives.

  Nucleosides, nucleotides & nucleic acids 20050101

• Determination of acidity constants of enolisable compounds by capillary electrophoresis.

  Analytical and bioanalytical chemistry 20041001

• Nitrosation of glycine ethyl ester and ethyl diazoacetate to give the alkylating agent and mutagen ethyl chloro(hydroximino)acetate.

  Chemical research in toxicology 20040301

• Facile synthesis of alpha,alpha-diisobutylglycine and anchoring its derivatives onto PAL-PEG-PS resin.

  The Journal of organic chemistry 20031212

• Sterically hindered C(alpha, alpha)-disubstituted alpha-amino acids: synthesis from alpha-nitroacetate and incorporation into peptides.

  The Journal of organic chemistry 20011019