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Key Documents

453137

Sigma-Aldrich

3,5-Dibromo-4-hydroxybenzaldehyde

98%

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About This Item

Linear Formula:
Br2C6H2(OH)CHO
CAS Number:
Molecular Weight:
279.91
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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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An expeditious synthesis of syringaldehyde from para-cresol.
Tripathi AK, et al.
Indian J. Chem. B, 49(3), 379-379 (2010)
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
Synthesis of 3, 4, 5-Trimethoxybenzaldehyde.
Manchand PS, et al.
Synthetic Communications, 20(17), 2659-2666 (1990)
Mengting Yang et al.
Environmental science & technology, 47(19), 10868-10876 (2013-09-13)
Using seawater for toilet flushing may introduce high levels of bromide and iodide into a city's sewage treatment works, and result in the formation of brominated and iodinated disinfection byproducts (DBPs) during chlorination to disinfect sewage effluents. In a previous
Shaoyang Hu et al.
Chemosphere, 228, 668-675 (2019-05-10)
As the first identified category of disinfection byproducts (DBPs), trihalomethanes (THMs) have received continuous attention. Previous studies have demonstrated that the transformation of aromatic halogenated DBPs during chlor (am)ination resulted in the formation of THMs, which may occur in both

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