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M80806

Sigma-Aldrich

4-Methylstyrene

96%, contains 3,5-di-tert-butylcatechol as inhibitor

Sinônimo(s):

4-Vinyltoluene

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About This Item

Fórmula linear:
CH3C6H4CH=CH2
Número CAS:
622-97-9
Peso molecular:
118.18
Beilstein:
1209317
Número CE:
210-762-8
Número MDL:
MFCD00008621
Código UNSPSC:
12162002
ID de substância PubChem:
24897220
NACRES:
NA.23

pressão de vapor

<1 mmHg ( 20 °C)

Ensaio

96%

Formulário

liquid

temperatura de autoignição

959 °F

contém

3,5-di-tert-butylcatechol as inhibitor

Lim. expl.

5.3 %

índice de refração

n20/D 1.542 (lit.)

p.e.

170-175 °C (lit.)

densidade

0.897 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Cc1ccc(C=C)cc1

InChI

1S/C9H10/c1-3-9-6-4-8(2)5-7-9/h3-7H,1H2,2H3

chave InChI

JLBJTVDPSNHSKJ-UHFFFAOYSA-N

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Descrição geral

4-Methylstyrene is a molecule with an extended Π conjugation. The threefold symmetric torsional potential of 4-methylstyrene has been investigated. Polymerization of 4-methylstyrene by employing a half-metallocene type catalytic system composed of (trimethyl)pentamethylcyclopentadienyltitanium (Cp*TiMe3), trioctylaluminum (AlOct3), and tris(pentafluorophenyl)borane [B(C6F5)3] has been reported. Palladium-catalyzed Heck coupling of chlorobenzene with 4-methylstyrene has been investigated.

Aplicação

4-Methylstyrene was employed as Π ligand in the preparation of cationic, two-coordinate triphenylphosphine-gold(I)-Π complexes.

Palavra indicadora

Danger

Frases de perigo

H226,H304,H411

Classificações de perigo

Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

113.0 °F

Ponto de fulgor (°C)

45 °C

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
MKCH7847
MKCF1120
MKBV6244V
MKBK0953V
S27997

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4-Cyanostyrene AldrichCPR

Sigma-Aldrich

CDS000773

4-Cyanostyrene

Methylstyrene (mixture of 3- and 4-isomers) stabilised with 4-tert-butylpyrocatechol for synthesis

Sigma-Aldrich

8.22098

Methylstyrene

2,4,6-Trimethylstyrene 95%, contains &lt;0.05% tert-butylcatechol as inhibitor

Sigma-Aldrich

259780

2,4,6-Trimethylstyrene

Rajeev K Sinha et al.
The Journal of chemical physics, 124(14), 144316-144316 (2006-04-22)
To understand the effect of the para position vinyl group substitution in toluene on methyl torsion, we investigated 4-methylstyrene, a benchmark molecule with an extended pi conjugation. The assignment for a 33 cm(-1) band in the excitation spectrum to the
Rachel E M Brooner et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(25), 8276-8284 (2013-04-18)
Cationic, two-coordinate triphenylphosphine-gold(I)-π complexes of the form [(PPh₃)Au(π ligand)]⁺SbF₆⁻ (π ligand=4-methylstyrene, 1∙SbF₆), 2-methyl-2-butene (3∙SbF₆), 3-hexyne (6∙SbF₆), 1,3-cyclohexadiene (7∙SbF₆), 3-methyl-1,2-butadiene (8∙SbF₆), and 1,7-diphenyl-3,4-heptadiene (10∙SbF₆) were generated in situ from reaction of [(PPh₃)AuCl], AgSbF₆, and π ligand at -78 °C and were
An efficient palladium-catalyzed Heck coupling of aryl chlorides with alkenes.
Yi C and Hua R.
Tetrahedron Letters, 47(15), 2573-2576 (2006)
Syndiospecific living polymerization of 4-methylstyrene and styrene with (trimethyl) pentamethylcyclopentadienyltitanium/tris (pentafluorophenyl) borane/trioctylaluminum catalytic system.
Kawabe M and Murata M.
Journal of Polymer Science Part A: Polymer Chemistry, 39(21), 3692-3706 (2001)
T Kühler
Xenobiotica; the fate of foreign compounds in biological systems, 14(5), 417-428 (1984-05-01)
N-Acetyl-L-cysteine was reacted with 2-(2-, 3-, or 4-methylphenyl)-oxiranes to give mixtures of the two possible regio isomers N-acetyl-S-[1-(2-, 3-, or 4-methylphenyl)-2-hydroxyethyl]-L-cysteine and N-acetyl-S-[2-(2-, 3-, or 4-methylphenyl)-2-hydroxyethyl]-L-cysteine, respectively. These were isolated in pure form by h.p.l.c.. The diastereomers were characterized by

Artigos

Heck Reaction

The Heck reaction is the palladium catalyzed cross-coupling reaction between alkenes and aryl or vinyl halides (or triflates) to afford substituted alkenes.

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