1-Bromo-4-tert-butylbenzene

Names

[ Name ]:
1-Bromo-4-tert-butylbenzene

[Synonym ]:
p-Bromo-tert-butylbenzene
4-tert-Butylbromobenzene
Benzene, 1-bromo-4-(1,1-dimethylethyl)-
MFCD00000108
1-Bromo-4-(2-methyl-2-propanyl)benzene
p-Bromo-t-butylbenzene
p-tert-butyl bromo benzene
1-Bromo-4-tert-butylbenzene
4-bromo-1-tert-butylbenzene
1-Bromo-4-(tert-butyl)benzene
EINECS 223-599-2
Butylbromobenzene
1-BROMO-p-t-BUTYLBENZENE
4-Bromo-tert-butylbenzene
4-t-Butylbromobenzene

Biological Activity

[Description]:

1-Bromo-4-tert-butylbenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

1-Bromo-4-tert-butylbenzene 用于合成 4-tert-butyl-phenylboronic acid1、CP-47,497 的 1-deoxy 类似物 (n = 0 to 7) 和 CP-55,940 的 1-deoxy 类似物 (n = 0 到 7）。它在 0°C 下在各种溶剂中与正丁基锂和叔丁基锂进行溴化锂交换反应。

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
232.0±9.0 °C at 760 mmHg

[ Melting Point ]:
13-16 °C(lit.)

[ Molecular Formula ]:
C₁₀H₁₃Br

[ Molecular Weight ]:
213.11

[ Flash Point ]:
97.2±0.0 °C

[ Exact Mass ]:
212.020050

[ LogP ]:
4.68

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.519

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S23-S24/25-S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29036990

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940.

Bioorg. Med. Chem. 16 , 322-35, (2008)

A series of 1-deoxy analogs of CP-47,497 (8 and 13, n=0-7) and 1-deoxy analogs of CP-55,940 (9, n=0-7) have been synthesized and their affinities for the cannabinoid CB(1) and CB(2) receptors have bee...

Effect of solvent on the lithium-bromine exchange of aryl bromides: reactions of n-butyllithium and tert-butyllithium with 1-bromo-4-tert-butylbenzene at 0 degrees C.

J. Org. Chem. 71(7) , 2825-8, (2006)

The outcome of reactions of 1-bromo-4-tert-butylbenzene (1), a representative aryl bromide, with n-BuLi or t-BuLi at 0 degrees C in a variety of solvent systems has been investigated. The products of ...

Novel non-symmetric nickel-diimine complexes for the homopolymerization of ethene: Control of branching by catalyst design. Schmid M, et al.

Z. Naturforsch. B 57(10) , 1141-46, (2002)