453137
3,5-Dibromo-4-hydroxybenzaldehyde
98%
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About This Item
Linear Formula:
Br2C6H2(OH)CHO
CAS Number:
Molecular Weight:
279.91
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
221-017-1
MDL number:
Assay:
98%
Quality Level
assay
98%
mp
181-185 °C (lit.)
functional group
aldehyde, bromo
SMILES string
Oc1c(Br)cc(C=O)cc1Br
InChI
1S/C7H4Br2O2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H
InChI key
SXRHGLQCOLNZPT-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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An expeditious synthesis of syringaldehyde from para-cresol.
Tripathi AK, et al.
Indian J. Chem. B, 49(3), 379-379 (2010)
Synthesis of 3, 4, 5-Trimethoxybenzaldehyde.
Manchand PS, et al.
Synthetic Communications, 20(17), 2659-2666 (1990)
Huirong Zhang et al.
PloS one, 12(10), e0185783-e0185783 (2017-10-04)
Sexually transmitted Chlamydia trachomatis is an extremely common infection and often leads to serious complications including infertility and pelvic inflammatory syndrome. Several broad-spectrum antibiotics are currently used to treat C. trachomatis. Although effective, they also kill beneficial vaginal lactobacilli. Two