116-11-0 | 2-Methoxypropene

Packsize	Purity	Availability	Price	Discounted Price
500mg	95%	in stock	$28.00	$19.00
1g	95%	in stock	$33.00	$23.00
2.5g	95%	in stock	$35.00	$24.00
5g	95%	in stock	$36.00	$25.00
50g	95%	in stock	$60.00	$42.00

Description

• Catalog Number: AA22393
• Chemical Name: 2-Methoxypropene
• CAS Number: 116-11-0
• Molecular Formula: C4H8O
• Molecular Weight: 72.10571999999999
• MDL Number: MFCD00014929
• SMILES: COC(=C)C

Computed Properties

• Complexity: 38.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

1-Propene, 2-methoxy- is a versatile chemical compound commonly used in various chemical synthesis applications. This particular molecule serves as a key building block in the creation of a wide range of products, thanks to its unique structure and reactivity. In chemical synthesis, 1-Propene, 2-methoxy- is utilized as a valuable intermediate in the production of pharmaceuticals, agrochemicals, fragrances, and other specialty chemicals. Its functional groups and molecular properties make it an important precursor in organic reactions, allowing for the creation of complex molecular structures with high efficiency and precision. This compound plays a crucial role in the development of new materials and compounds, showcasing its significance in the field of chemical synthesis.

Literature

• Glycosyl hydroperoxides derived from 2-deoxysugars.

  Carbohydrate research 20101122

• Acetonation of L-pentoses and 6-deoxy-L-hexoses under kinetic control using heterogeneous acid catalysts.

  Carbohydrate research 20100719

• Preparation of pure lipid hydroperoxides.

  Journal of lipid research 20081201

• Identification of the aromatic tertiary N-oxide functionality in protonated analytes via ion/molecule reactions in mass spectrometers.

  The Journal of organic chemistry 20080704

• Mechanism and chemoselectivity of the Pd(II)-catalyzed allylation of aldehydes: a density functional theory study.

  The Journal of organic chemistry 20070202

• Exclusive formation of alpha-methyleneoxetanes in ketene-alkene cycloadditions. Evidence for intervention of both an alpha-methyleneoxetane and the subsequent 1,4-zwitterion.

  Journal of the American Chemical Society 20031126

• Asymmetric catalysis of hetero-ene reactions with tridentate Schiff base chromium(III) complexes.

  Journal of the American Chemical Society 20020327

• Mixed acetals of cyclodextrins. Preparation of hexakis-, heptakis- and octakis[2,6-di-O-(methoxydimethyl)methyl]-alpha-, beta- and gamma-cyclodextrins.

  Carbohydrate research 20020205

• A new mixed acetal-type substitution pattern for alpha-cyclodextrin. Preparation of hexakis (3-O-benzyl)- alpha-cyclodextrin.

  Carbohydrate letters 20010101