Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H16 |
| Molecular Weight | 148.2447 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C=C1)C(C)(C)C
InChI
InChIKey=QCWXDVFBZVHKLV-UHFFFAOYSA-N
InChI=1S/C11H16/c1-9-5-7-10(8-6-9)11(2,3)4/h5-8H,1-4H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Tetra-kis(4-tert-butyl-benz-yl)silane. | 2010-08-28 |
|
| Concise synthesis of two natural triterpenoid saponins, oleanolic acid derivatives isolated from the roots of Pulsatilla chinensis. | 2009-07-27 |
|
| Synthesis and anti-HIV activity evaluation of novel 2,4-disubstituted 7-methyl-1,1,3-trioxo-2,4-dihydro-pyrazolo-[4,5-e][1,2]thiadiazines. | 2008-04 |
|
| Dramatic acceleration of the Menschutkin reaction and distortion of halide leaving-group order. | 2007-12-07 |
|
| Environmental green chemistry as defined by photocatalysis. | 2007-07-31 |
|
| Synthesis, structure, and activity of supramolecular mimics for the active site and arg141 residue of copper, zinc-superoxide dismutase. | 2007-02-05 |
|
| [Determination of p-tert-butyl toluene in air of working places with gas chromatography]. | 2007-02 |
|
| Partial oxidation of 4-tert-butyltoluene catalyzed by homogeneous cobalt and cerium acetate catalysts in the Br-/H2O2/acetic acid system: insights into selectivity and mechanism. | 2007 |
|
| Arylthiolate-protected silver quantum dots. | 2006-12-19 |
|
| Comparative in vivo behavior studies of cyclen-based copper-64 complexes: regioselective synthesis, X-ray structure, radiochemistry, log P, and biodistribution. | 2004-12-16 |
|
| N-4-methansulfonamidobenzyl-N'-2-substituted-4-tert-butyl-benzyl thioureas as potent vanilloid receptor antagonistic ligands. | 2004-04-05 |
|
| N-[4-(methylsulfonylamino)benzyl]thiourea analogues as vanilloid receptor antagonists: analysis of structure-activity relationships for the "C-Region". | 2004-01-15 |
|
| N-(3-acyloxy-2-benzylpropyl)-N'-[4-(methylsulfonylamino)benzyl]thiourea analogues: novel potent and high affinity antagonists and partial antagonists of the vanilloid receptor. | 2003-07-03 |
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6589
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5008
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C027647
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202-675-9
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98-51-1
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SUBSTANCE RECORD
