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MilliporeSigma

114995

2′-Hydroxy-5′-methoxyacetophenone

99%

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About This Item

Linear Formula:
HOC6H3(OCH3)COCH3
CAS Number:
705-15-7
Molecular Weight:
166.17
NACRES:
NA.22
PubChem Substance ID:
24847194
UNSPSC Code:
12352100
EC Number:
211-882-3
MDL number:
MFCD00008731

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Product Name

2′-Hydroxy-5′-methoxyacetophenone, 99%

InChI key

MLIBGOFSXXWRIY-UHFFFAOYSA-N

InChI

1S/C9H10O3/c1-6(10)8-5-7(12-2)3-4-9(8)11/h3-5,11H,1-2H3

SMILES string

COc1ccc(O)c(c1)C(C)=O

assay

99%

form

solid

mp

52 °C (lit.)

λmax

355 nm

functional group

ketone

Quality Level

200

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This Item
543780630586IDF00131
2′-Hydroxy-5′-methoxyacetophenone 99%

Sigma-Aldrich

114995

2′-Hydroxy-5′-methoxyacetophenone

5′-Fluoro-2′-hydroxy-3′-nitroacetophenone 98%

Sigma-Aldrich

543780

5′-Fluoro-2′-hydroxy-3′-nitroacetophenone

2′-Hydroxy-4′,6′-dimethoxyacetophenone 97%

Sigma-Aldrich

630586

2′-Hydroxy-4′,6′-dimethoxyacetophenone

2-(3′,4′-Dimethoxyphenyl)-2′-hydroxy-4′-methoxyacetophenone AldrichCPR

Sigma-Aldrich

IDF00131

2-(3′,4′-Dimethoxyphenyl)-2′-hydroxy-4′-methoxyacetophenone

assay

99%

assay

98%

assay

97%

assay

-

form

solid

form

-

form

solid

form

solid

mp

52 °C (lit.)

mp

87-90 °C (lit.)

mp

80-84 °C (lit.)

mp

-

λmax

355 nm

λmax

-

λmax

-

λmax

-

functional group

ketone

functional group

fluoro, ketone, nitro

functional group

ketone

functional group

-

General description

2′-Hydroxy-5′-methoxyacetophenone is observed as a side reaction product of elbs persulphate oxidation of phenols[1].

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000506328
0000506328
0000252429
0000225506
0000221944

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463. The elbs persulphate oxidation of phenols, and its adaptation to the preparation of monoalkyl ethers of quinols.
Baker W and Brown NC.
Journal of the Chemical Society, 2303-2307 (1948)

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