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253928

Sigma-Aldrich

1-Bromo-4-tert-butylbenzene

97%

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About This Item

Linear Formula:
(CH3)3CC6H4Br
CAS Number:
3972-65-4
Molecular Weight:
213.11
Beilstein:
1859117
EC Number:
223-599-2
MDL number:
MFCD00000108
UNSPSC Code:
12352100
PubChem Substance ID:
24855340
NACRES:
NA.22

Quality Level

200

Assay

97%

form

liquid

refractive index

n20/D 1.533 (lit.)

bp

80-81 °C/2 mmHg (lit.)

mp

13-16 °C (lit.)

density

1.229 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccc(Br)cc1

InChI

1S/C10H13Br/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,1-3H3

InChI key

XHCAGOVGSDHHNP-UHFFFAOYSA-N

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General description

1-Bromo-4-tert-butylbenzene undergoes lithium-bromide exchange reactions with n-butyllithium and tert-butyllithium at 0°C in various solvents.

Application

1-Bromo-4-tert-butylbenzene was used in the synthesis of 4-tert-butyl-phenylboronic acid, 1-deoxy analogs of CP-47,497 (n = 0 to 7) and 1-deoxy analogs of CP-55,940 (n = 0 to 7).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

206.6 °F

Flash Point(C)

97 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Novel non-symmetric nickel-diimine complexes for the homopolymerization of ethene: Control of branching by catalyst design.
Schmid M, et al.
Zeitschrift fur Naturforschung, B: Chemical Sciences, 57(10), 1141-1146 (2002)
William F Bailey et al.
The Journal of organic chemistry, 71(7), 2825-2828 (2006-03-25)
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 reactions of 1 with n-BuLi vary significantly with changes
John W Huffman et al.
Bioorganic & medicinal chemistry, 16(1), 322-335 (2007-10-09)
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 been determined. Although the majority of these compounds
Xiao Yan et al.
Physical chemistry chemical physics : PCCP, 22(11), 6222-6230 (2020-03-05)
Unveiling the reaction mechanism is significant for developing high-performance catalysts. In this paper, a series of precisely controlled PdxM147-x (M = Cu, Pt, Au, Rh, Ru) dendrimer encapsulated nanoparticles (DENs) has been successfully synthesized. The mechanisms of PdxM147-x as catalysts

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