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Merck
CN

54590

4-Hydroxybenzaldehyde

≥95.0% (HPLC)

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About This Item

Linear Formula:
HOC6H4CHO
CAS Number:
Molecular Weight:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-599-1
Beilstein/REAXYS Number:
471352
MDL number:
Assay:
≥95.0% (HPLC)
Form:
solid
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Quality Level

assay

≥95.0% (HPLC)

form

solid

mp

112-116 °C (lit.)

functional group

aldehyde

SMILES string

[H]C(=O)c1ccc(O)cc1

InChI

1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H

InChI key

RGHHSNMVTDWUBI-UHFFFAOYSA-N

Application

4-Hydroxybenzaldehyde may be used as a reactant during the synthesis of 4-(4-hydroxyphenyl)-but-3-ene-2-one (a raspberry ketone precursor) and [(pyrrole-2,5-diyl)-co-(benzylidene)]. It may also be used to prepare nonlinear optical quinolinium single crystals (an OHQ–TMS compound) via a condensation reaction with 1,2-dimethylquinolinium 2,4,6-trimethylbenzenesulfonate in methanol.


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pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

345.2 °F

flash_point_c

174 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves



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New phenolic N-methylquinolinium single crystals for second-order nonlinear optics.
Kim JS, et al.
Opt. Mater., 45, 136-140 (2015)
Preparation of a raspberry ketone precursor in the presence of rare earth oxide catalysts.
Hoelderich WF and Ritzerfeld V.
Applied Catalysis A: General, 504, 654-663 (2015)
Secondary amide-based linkers for solid phase organic synthesis.
Swayze EE.
Tetrahedron Letters, 38(49), 8465-8468 (1997)



Global Trade Item Number

SKUGTIN
54590-50G-F04061832568416
54590-1KG-F04061825591803
54590-250G-F04061832568386