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Merck
CN

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%
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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



pictograms

Exclamation mark

signalword

Warning

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

Regulatory Information

新产品

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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
C Flodin et al.
Phytochemistry, 53(1), 77-80 (2000-02-03)
The red marine alga Polysiphonia sphaerocarpa was extracted by a simultaneous steam distillation-solvent extraction technique and several brominated compounds were identified by gas chromatography-mass spectrometry. The compounds detected were 2,4-dibromoanisole, 2,4,6-tribromoanisole, 3-bromocresol, 3,5-dibromocresol, 3-bromo-4-hydroxybenzaldehyde, 3,5-dibromo-4-hydroxybenzaldehyde, 2-bromophenol, 4-bromophenol, 2,4-dibromophenol, 2,6-dibromophenol and



Global Trade Item Number

SKUGTIN
516775-5G04061831830118