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About This Item
Empirical Formula (Hill Notation):
C6H7BrN2O2
CAS Number:
Molecular Weight:
219.04
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
mp
182-185 °C (lit.)
functional group
bromo
SMILES string
CN1C=C(Br)C(=O)N(C)C1=O
InChI
1S/C6H7BrN2O2/c1-8-3-4(7)5(10)9(2)6(8)11/h3H,1-2H3
InChI key
QITOSXPGCRFMDG-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
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L Celewicz
Journal of photochemistry and photobiology. B, Biology, 3(4), 565-574 (1989-08-01)
Photochemical reactions between 5-bromo-1,3-dimethyluracils and 3-substituted indoles in acetone solution were studied. Irradiation (lambda greater than 290 nm) of 5-bromo-1,3-dimethyluracil (1) and N alpha-acetyl-L-tryptophan methyl ester (2) yields, in addition to 5-(2-indolyl)uracil (3), a new photoadduct 5-(7-indolyl)uracil (4). 5-Bromo-1,3-dimethyluracils with
Ming-Juan Li et al.
The journal of physical chemistry. B, 117(39), 11660-11669 (2013-08-27)
The resonance Raman spectroscopic study of the excited state structural dynamics of 1,3-dimethyluracil (DMU), 5-bromo-1,3-dimethyluracil (5BrDMU), uracil, and thymine in water and acetonitrile were reported. Density functional theory calculations were carried out to help elucidate the ultraviolet electronic transitions associated
Photoinduced cross-coupling reaction of 5-bromo-1, 3-dimethyluracil to electron-rich aromatics.
Ito S, et al.
Tetrahedron, 37(1), 45-50 (1981)
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