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:
Molecular Weight:
199.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-793-5
MDL number:
Assay:
99%
Form:
solid
InChI key
SCZXFZRJDVZMJI-UHFFFAOYSA-N
InChI
1S/C9H11Br/c1-6-4-8(3)9(10)5-7(6)2/h4-5H,1-3H3
SMILES string
Cc1cc(C)c(Br)cc1C
assay
99%
form
solid
bp
233-235 °C (lit.)
mp
71-73 °C (lit.)
functional group
bromo
Quality Level
Related Categories
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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Synthesis of Ubiquinones Utilizing Pd (0)-Catalyzed Stille Coupling.
Jung YS, et al.
Bull. Korean Chem. Soc., 21(5), 463-464 (2000)
2, 4, 5-Trimethylbenzoic Acid.
Barcon A, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 53(12), 1842-1845 (1997)
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
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