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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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