| Identification | Back Directory | [Name]
GLYCOLALDEHYDE | [CAS]
141-46-8 | [Synonyms]
Diose
HOCH2CHO
Glycoaldehyde
GLYCOLALDEHYDE
hydroxyethanal
glycollaldehyde
2-hydroxyethanal
GLYCOLICALDEHYDE
hydroxy-acetaldehyd
Hydroxyacetaldehyde
methylolformaldehyde
2-hydroxyacetaldehyde
Methylol formaldehyde
Monomethylolformaldehyde
Acetaldehyde, hydroxy-(9CI)
141-46-8 GLYCOLALDEHYDE C2H4O2
Glycoaldehyde 2-Hydroxyacetaldehyde
Glycolaldehyde
DISCONTINUED. Please see G641150 | [EINECS(EC#)]
205-484-9 | [Molecular Formula]
C2H4O2 | [MDL Number]
MFCD00038088 | [MOL File]
141-46-8.mol | [Molecular Weight]
60.05 |
| Hazard Information | Back Directory | [Definition]
ChEBI: The glycolaldehyde derived from ethylene glycol. The parent of the class of glycolaldehydes. | [Hazard]
Moderately toxic by ingestion | [Uses]
Glycolaldehyde is derived from 2,2-Diethoxyethanol (D441940), which is used in the synthesis of neooxazolomycin, part of the oxazolomycin family of antibiotics. Also used in the synthesis of pyrimidine based inhibitors of phosphodiesterase 7 (PDE7). | [Synthesis]
Glycolaldehyde was prepared as follows: formaldehyde (30 mmol) was placed in a reactor, then N,N-dimethylformamide (10 ml) was added to the reactor, amidine catalyst I-K (0.15 mmol, as shown in FIG. 2) or silica gel solid-loaded triazole catalyst A-H ( |
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| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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