2,6-Di-tert-butyl-4-methylpyridine - CAS 38222-83-2
Catalog: |
BB023586 |
Product Name: |
2,6-Di-tert-butyl-4-methylpyridine |
CAS: |
38222-83-2 |
Synonyms: |
2,6-ditert-butyl-4-methylpyridine |
IUPAC Name: | 2,6-ditert-butyl-4-methylpyridine |
Description: | 2,6-Di-tert-butyl-4-methylpyridine (CAS# 38222-83-2) is used as a catalyst in the rapid assembly of complex oligosaccharides. Also a catalyst for the stereoselective construction of C(20) in steroidal derivatives in the synthesis of epimeric structural analogs in pharmaceuticals. |
Molecular Weight: | 205.34 |
Molecular Formula: | C14H23N |
Canonical SMILES: | CC1=CC(=NC(=C1)C(C)(C)C)C(C)(C)C |
InChI: | InChI=1S/C14H23N/c1-10-8-11(13(2,3)4)15-12(9-10)14(5,6)7/h8-9H,1-7H3 |
InChI Key: | HVHZEKKZMFRULH-UHFFFAOYSA-N |
Boiling Point: | 233 °C |
Melting Point: | 33-36 °C |
Purity: | 95 % |
Density: | 1.476 g/cm3 |
Appearance: | Light yellow powder |
Storage: | 2-8 °C |
MDL: | MFCD00006305 |
LogP: | 3.98500 |
GHS Hazard Statement: | H302 (88.64%): 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 |
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PMID | Publication Date | Title | Journal |
19582903 | 20090701 | PIKfyve regulation of endosome-linked pathways | Traffic (Copenhagen, Denmark) |
18528988 | 20080702 | Stereoselective direct glycosylation with anomeric hydroxy sugars by activation with phthalic anhydride and trifluoromethanesulfonic anhydride involving glycosyl phthalate intermediates | Journal of the American Chemical Society |
17078715 | 20061109 | Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives | Organic letters |
15941236 | 20050615 | One-step synthesis of triethynylvinylmethanes and tetraethynylmethanes by GaCl(3)-promoted diethynylation of 1,4-enynes and 1,4-diynes | Journal of the American Chemical Society |
15357594 | 20040917 | Stereoselective synthesis of allyl-C-mannosyl compounds: use of a temporary silicon connection in intramolecular allylation strategies with allylsilanes | The Journal of organic chemistry |
Complexity: | 184 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 205.183049738 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 205.183049738 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 4.6 |
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