2,4,6-Tri-tert-butylpyrimidine - CAS 67490-21-5
Catalog: |
BB033294 |
Product Name: |
2,4,6-Tri-tert-butylpyrimidine |
CAS: |
67490-21-5 |
Synonyms: |
2,4,6-tritert-butylpyrimidine |
IUPAC Name: | 2,4,6-tritert-butylpyrimidine |
Description: | 2,4,6-Tri-tert-butylpyrimidine (CAS# 67490-21-5) is a useful research chemical compound. |
Molecular Weight: | 248.41 |
Molecular Formula: | C16H28N2 |
Canonical SMILES: | CC(C)(C)C1=CC(=NC(=N1)C(C)(C)C)C(C)(C)C |
InChI: | InChI=1S/C16H28N2/c1-14(2,3)11-10-12(15(4,5)6)18-13(17-11)16(7,8)9/h10H,1-9H3 |
InChI Key: | VYWSYEDVFVGRGG-UHFFFAOYSA-N |
Boiling Point: | 292.2 °C at 760 mmHg |
Density: | 0.9 g/cm3 |
Appearance: | White to tan powder or crystals |
MDL: | MFCD03094045 |
LogP: | 4.36910 |
Publication Number | Title | Priority Date |
CN-110746471-A | Preparation method of fondaparinux sodium disaccharide intermediate | 20191104 |
CN-110746471-B | Preparation method of fondaparinux sodium disaccharide intermediate | 20191104 |
US-2020235306-A1 | Organic compound and organic electroluminescence device using the same | 20190120 |
US-2020216573-A1 | Expedient synthesis of core disaccharide building blocks from natural polysaccharides for heparan sulfate oligosaccharide assembly | 20181221 |
WO-2020103118-A1 | Process for producing substituted anthraquinone | 20181123 |
PMID | Publication Date | Title | Journal |
21070063 | 20101217 | Influence of the O3 protecting group on stereoselectivity in the preparation of C-mannopyranosides with 4,6-O-benzylidene protected donors | The Journal of organic chemistry |
19924835 | 20091218 | Highly stereoselective synthesis of alpha-D-mannopyranosyl phosphosugars | The Journal of organic chemistry |
12605514 | 20030306 | Direct synthesis of the beta-l-rhamnopyranosides | Organic letters |
12137540 | 20020731 | Solid-phase synthesis of beta-mannosides | Journal of the American Chemical Society |
11552809 | 20010919 | 1-Benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride: a potent combination of shelf-stable reagents for the low-temperature conversion of thioglycosides to glycosyl triflates and for the formation of diverse glycosidic linkages | Journal of the American Chemical Society |
Complexity: | 253 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 248.225248902 |
Formal Charge: | 0 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 248.225248902 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 25.8 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 5.3 |
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