![]() 2-C-Methyl-D-erythritol structure
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Common Name | 2-C-Methyl-D-erythritol | ||
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CAS Number | 58698-37-6 | Molecular Weight | 136.14600 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C5H12O4 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A |
Metabolic engineering of Bacillus subtilis for terpenoid production.
Appl. Microbiol. Biotechnol. 99 , 9395-406, (2015) Terpenoids are the largest group of small-molecule natural products, with more than 60,000 compounds made from isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP). As the most diverse group of small-molecule natural products, terpen... |
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Formation of secondary organic aerosols through photooxidation of isoprene.
Science 303 , 1173-1176, (2004) Detailed organic analysis of natural aerosols from the Amazonian rain forest showed considerable quantities of previously unobserved polar organic compounds, which were identified as a mixture of two diastereoisomeric 2-methyltetrols: 2-methylthreitol and 2-m... |
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Water-soluble constituents of ajowan.
Chem. Pharm. Bull. 49 , 840—844, (2001) From the water-soluble portion of the methanol extract of the fruit of Carum ajowan (ajowan), which has been used as a spice and medicine, 25 compounds, including five new monoterpenoid glucosides, a new monoterpenoid, two new aromatic compound glucosides, an... |
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2-C-methyl-D-erythritol is a major carbohydrate in petals of Phlox subulata possibly involved in flower development.
J. Plant Physiol. 161 , 977-980, (2004) 2-C-methyl-D-erythritol, a soluble carbohydrate that is not ubiquitously found in higher plants, was detected in the ethanol extract from Phlox subulata petals and isolated using HPLC. The isolated compound was identified by 1H-NMR, 13C-NMR and Cl-MS spectra.... |
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Biosynthesis of 2-C-methyl-D-erythritol, a putative C5 intermediate in the mevalonate independent pathway for isoprenoid biosynthesis. Duvold, T., et al.
Tetrahedron Lett. 38 , 4769-4772, (1997)
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Incorporation of 2-C-methyl-D-erythritol, a putative isoprenoid precursor in the mevalonate-independent pathway, into ubiquinone and menaquinone of Escherichia coli. Duvold, T., et al.
Tetrahedron Lett. 38 , 6181-6184, (1997)
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