Glycolaldehyde dimer - CAS 23147-58-2
Catalog: |
BB017951 |
Product Name: |
Glycolaldehyde dimer |
CAS: |
23147-58-2 |
Synonyms: |
1,4-dioxane-2,5-diol |
IUPAC Name: | 1,4-dioxane-2,5-diol |
Description: | Glycolaldehyde dimer (CAS# 23147-58-2) is derivative of glcoaldehyde, which is the precursor molecule of various significant compounds including amino acid glycine and in the formose reaction. |
Molecular Weight: | 120.10 |
Molecular Formula: | C4H8O4 |
Canonical SMILES: | C1C(OCC(O1)O)O |
InChI: | InChI=1S/C4H8O4/c5-3-1-7-4(6)2-8-3/h3-6H,1-2H2 |
InChI Key: | ATFVTAOSZBVGHC-UHFFFAOYSA-N |
Boiling Point: | 110~ 120 °C (1.6kPa ) |
Purity: | 98 % |
Density: | 1.455 g/cm3 |
Appearance: | White powder |
MDL: | MFCD00012133 |
LogP: | -1.33000 |
GHS Hazard Statement: | H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113416177-A | Main chain degradable photoresist resin monomer and preparation method and application thereof | 20210624 |
JP-2021136920-A | Antibodies to advanced glycation end products and their use | 20200304 |
CN-111004291-A | Etimicin derivative and synthetic method thereof | 20191219 |
WO-2021106988-A1 | G9a INHIBITOR | 20191127 |
CN-110590733-A | Synthesis method of 1,4-dioxane-2,5-diol | 20190929 |
PMID | Publication Date | Title | Journal |
19449841 | 20090703 | Synthesis of Passerini-Ugi hybrids by a four-component reaction using the glycolaldehyde dimer | The Journal of organic chemistry |
18155175 | 20080201 | Glycated human serum albumin enhances macrophage inflammatory protein-1beta mRNA expression through protein kinase C-delta and NADPH oxidase in macrophage-like differentiated U937 cells | Biochimica et biophysica acta |
12735984 | 20030529 | Synthesis of 9-oxime-11,12-carbamate ketolides through a novel N-deamination reaction of 11,12-hydrazonocarbamate ketolide | Bioorganic & medicinal chemistry |
12123075 | 20020507 | The in situ oxidation-Wittig reaction of alpha-hydroxyketones | Chemical communications (Cambridge, England) |
11784164 | 20011227 | An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction | Organic letters |
Complexity: | 64.4 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 120.04225873 |
Formal Charge: | 0 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 120.04225873 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 58.9 Å2 |
Undefined Atom Stereocenter Count: | 2 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -1.3 |
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