trans-3-(tert-Butyldimethylsilyloxy)-N,N-dimethyl-1,3-butadien-1-amine - CAS 194233-66-4
Catalog: |
BB015041 |
Product Name: |
trans-3-(tert-Butyldimethylsilyloxy)-N,N-dimethyl-1,3-butadien-1-amine |
CAS: |
194233-66-4 |
Synonyms: |
(1E)-3-[tert-butyl(dimethyl)silyl]oxy-N,N-dimethylbuta-1,3-dien-1-amine |
IUPAC Name: | (1E)-3-[tert-butyl(dimethyl)silyl]oxy-N,N-dimethylbuta-1,3-dien-1-amine |
Description: | trans-3-(tert-Butyldimethylsilyloxy)-N,N-dimethyl-1,3-butadien-1-amine (CAS# 194233-66-4) is a useful research chemical. |
Molecular Weight: | 227.42 |
Molecular Formula: | C12H25NOSi |
Canonical SMILES: | CC(C)(C)[Si](C)(C)OC(=C)C=CN(C)C |
InChI: | InChI=1S/C12H25NOSi/c1-11(9-10-13(5)6)14-15(7,8)12(2,3)4/h9-10H,1H2,2-8H3/b10-9+ |
InChI Key: | NSCKABIMFIKUEF-MDZDMXLPSA-N |
Boiling Point: | 234 °C (lit.) |
Density: | 0.878 g/mL at 25°C(lit.) |
Appearance: | Colorless to orange to brown liquid |
MDL: | MFCD01863582 |
LogP: | 3.59720 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
EP-3212618-A1 | Inhibitors of the renal outer medullary potassium channel | 20141031 |
EP-3212618-B1 | Inhibitors of the renal outer medullary potassium channel | 20141031 |
US-2017275283-A1 | Inhibitors of the renal outer medullary potassium channel | 20141031 |
US-9850245-B2 | Inhibitors of the renal outer medullary potassium channel | 20141031 |
WO-2016065602-A1 | Inhibitors of renal outer medullary potassium channel | 20141031 |
PMID | Publication Date | Title | Journal |
22397369 | 20120406 | Scalable synthesis of highly reactive 1,3-diamino dienes from vinamidinium salts and their use in Diels-Alder reactions | The Journal of organic chemistry |
22424074 | 20120328 | Cationic iron(III) porphyrin-catalyzed [4 + 2] cycloaddition of unactivated aldehydes with simple dienes | Journal of the American Chemical Society |
20024206 | 20091221 | Highly enantioselective hetero-Diels-Alder reactions between Rawal's diene and aldehydes catalyzed by chiral dirhodium(II) carboxamidates | Chemical communications (Cambridge, England) |
17249797 | 20070201 | Hydrogen bonding catalysis operates by charge stabilization in highly polar Diels-Alder reactions | Organic letters |
16095303 | 20050819 | Sequential aminodiene Diels-Alder approach to the ergoline skeleton | The Journal of organic chemistry |
Complexity: | 249 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 227.170540955 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 227.170540955 |
Rotatable Bond Count: | 5 |
Topological Polar Surface Area: | 12.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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