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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
Structure of 4-TERT-BUTYLTOLUENE

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

HIDE SMILES / InChI

Molecular Formula C11H16
Molecular Weight 148.2447
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
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
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:49:13 GMT 2025
Edited
by admin
on Mon Mar 31 20:49:13 GMT 2025
Record UNII
589519D43L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-TERT-BUTYLTOLUENE
Systematic Name English
4-T-BUTYLTOLUENE
HSDB  
Preferred Name English
TBT
Common Name English
4-T-BUTYLTOLUENE [HSDB]
Common Name English
TOLUENE, P-TERT-BUTYL-
Common Name English
1-(1,1-DIMETHYLETHYL)-4-METHYLBENZENE
Systematic Name English
1-TERT-BUTYL-4-METHYLBENZENE
Systematic Name English
1-METHYL-4-(2-METHYL-2-PROPANYL)BENZENE
Systematic Name English
NSC-6589
Code English
Code System Code Type Description
NSC
6589
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
HSDB
5008
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
PUBCHEM
7390
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
FDA UNII
589519D43L
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
MESH
C027647
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-675-9
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID1024704
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY
CAS
98-51-1
Created by admin on Mon Mar 31 20:49:13 GMT 2025 , Edited by admin on Mon Mar 31 20:49:13 GMT 2025
PRIMARY