Ethylenediamine diacetate - CAS 38734-69-9
Catalog: |
BB023736 |
Product Name: |
Ethylenediamine diacetate |
CAS: |
38734-69-9 |
Synonyms: |
acetic acid;ethane-1,2-diamine |
IUPAC Name: | acetic acid;ethane-1,2-diamine |
Description: | Ethylenediamine diacetate (CAS# 38734-69-9) is used as a catalyst for the preparation of various organic compounds such as methanodibenzodioxocin flavonoids, and chromeno-annulated cis-fused pyrano[3,4-c]benzopyran. It is also useful reagent for the synthesis of organic compunds such as arylmethyl nitrodihydroimidazopyridinium. |
Molecular Weight: | 180.20 |
Molecular Formula: | C6H16N2O4 |
Canonical SMILES: | CC(=O)O.CC(=O)O.C(CN)N |
InChI: | InChI=1S/C2H8N2.2C2H4O2/c3-1-2-4;2*1-2(3)4/h1-4H2;2*1H3,(H,3,4) |
InChI Key: | SAXQBSJDTDGBHS-UHFFFAOYSA-N |
Boiling Point: | 119.7 ℃ at 760 mmHg |
Appearance: | White powder, crystals, crystalline powder, flakes and/or chunks |
MDL: | MFCD00192147 |
LogP: | 0.48620 |
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PMID | Publication Date | Title | Journal |
22929231 | 20121001 | Ethylenediamine diacetate (EDDA) mediated synthesis of aurones under ultrasound: their evaluation as inhibitors of SIRT1 | Bioorganic & medicinal chemistry letters |
18442292 | 20080606 | Concise total synthesis of biologically interesting mallotophilippens C and e | The Journal of organic chemistry |
17909497 | 20070712 | An efficient and rapid synthetic route to biologically interesting pyranochalcone natural products | Molecules (Basel, Switzerland) |
Complexity: | 37 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 3 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 180.111007 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 4 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 180.111007 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 127 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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