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211419

5-Bromo-1,2,4-trimethylbenzene

99%

Synonym(s):

5-Bromopseudocumene

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About This Item

Linear Formula:
BrC6H2(CH3)3
CAS Number:
5469-19-2
Molecular Weight:
199.09
NACRES:
NA.22
PubChem Substance ID:
24852685
UNSPSC Code:
12352100
EC Number:
226-793-5
MDL number:
MFCD00000072
Assay:
99%
Form:
solid
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Quality Level

100

assay

99%

form

solid

bp

233-235 °C (lit.)

mp

71-73 °C (lit.)

functional group

bromo

SMILES string

Cc1cc(C)c(Br)cc1C

InChI

1S/C9H11Br/c1-6-4-8(3)9(10)5-7(6)2/h4-5H,1-3H3

InChI key

SCZXFZRJDVZMJI-UHFFFAOYSA-N

Application

5-Bromo-1,2,4-trimethylbenzene was used in the preparation of:
  • 1′,2′-dideoxy-1′-(1,2,4-trimethylphenyl)-3′,5′-di-O-toluoyl-β-D-ribofuranose
  • ubiquinones, also referred as Coenzyme Qn
  • 2, 4, 5-trimethylbenzoic acid

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP5463
MKCL7419
MKCJ8885
MKBW6334V
MKBS4469V

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2, 4, 5-Trimethylbenzoic Acid.
Barcon A, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 53(12), 1842-1845 (1997)
Synthesis of Ubiquinones Utilizing Pd (0)-Catalyzed Stille Coupling.
Jung YS, et al.
Bull. Korean Chem. Soc., 21(5), 463-464 (2000)
Barbara A Schweitzer et al.
The Journal of organic chemistry, 59(24), 7238-7242 (1994-12-01)
Described are the design, synthesis, and structures of three nonpolar nucleoside isosteres to be used as probes of noncovalent bonding in DNA and as isosteric replacements for the natural nucleosides in designed nucleic acid structures. Reaction of substituted aryl Grignards

Global Trade Item Number

SKUGTIN
211419-100G04061832685564