516775
3-Bromo-4-hydroxybenzaldehyde
97%
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About This Item
Linear Formula:
BrC6H3(OH)CHO
CAS Number:
Molecular Weight:
201.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Segment
assay
97%
mp
130-135 °C (lit.)
functional group
aldehyde, bromo
SMILES string
Oc1ccc(C=O)cc1Br
InChI
1S/C7H5BrO2/c8-6-3-5(4-9)1-2-7(6)10/h1-4,10H
InChI key
UOTMHAOCAJROQF-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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Related Content
Hard acid and soft nucleophile system. New efficient method for removal of benzyl protecting group.
Fuji K, et al.
The Journal of Organic Chemistry, 44(10), 1661-1664 (1979)
S L Manley et al.
Plant physiology, 64(6), 1032-1038 (1979-12-01)
The biosynthesis of 4-hydroxybenzaldehyde and 3-bromo-4-hydroxybenzaldehyde from l-[U-(14)C]tyrosine has been demonstrated in chloroplast-containing fractions obtained by differential and isopycnic centrifugation from the marine red alga Odonthalia floccosa. Surfactant and high speed centrifugation studies indicate that the biosynthetic pathway involves a
Formation of 3-bromo-4-hydroxybenzaldehyde from L-tyrosine in cell-free homogenates of Odonthalia floccosa (Rhodophyceae): a proposed biosynthetic pathway for brominated phenols.
Manley SL and Chapman DJ.
Febs Letters, 93(1), 97-101 (1978)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 516775-5G | 04061831830118 |