Methyl acetoacetate undergoes asymmetric hydrogenation to form (R)-(-)-methyl-3-hydroxybutyrate in the presence of enantioselective Ni/SiO2 catalysts. It undergoes Pechmann reactions with phenols in various ionic liquids.Methyl acetoacetate was used in development of a simple and cost effective method for monitoring of trace formaldehyde in air. It was used to study the substrate specificity of NADPH-dependent diacetyl reductase in Escherichia coli. Specification: Standard for GC,≥99.5%(GC) MDL Number: MFCD00008784 Molecular Formula: C5H8O3 Molecular Weight: 116.12 EC Number: 203-299-8 PubChem CID: 7757 Isomeric SMILES: CC(=O)CC(=O)OC Beilstein Registry Number: 506727 Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/M108601-SCI_5ea839d6db8d76e27121196048bcef13.pdf
- UPC:
- 12352211
- Condition:
- New
- Availability:
- 2 weeks
- Weight:
- 1.30 Ounces
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- M108601-5ml
- CAS:
- 105-45-3
- Product Size:
- 5ml
- Hazard Statement Codes:
- H227:H303:H316:H319
- Precautionary Statement Codes:
- P305+P351+P338
