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Merck
CN

265160

3,4-Difluorobenzaldehyde

97%

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About This Item

Linear Formula:
F2C6H3CHO
CAS Number:
34036-07-2
Molecular Weight:
142.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856058
EC Number:
422-180-3
Beilstein/REAXYS Number:
2241231
MDL number:
MFCD00010328

Key Documents

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Product Name

3,4-Difluorobenzaldehyde, 97%

InChI key

JPHKMYXKNKLNDF-UHFFFAOYSA-N

InChI

1S/C7H4F2O/c8-6-2-1-5(4-10)3-7(6)9/h1-4H

SMILES string

[H]C(=O)c1ccc(F)c(F)c1

assay

97%

form

liquid

refractive index

n20/D 1.5 (lit.)

density

1.288 g/mL at 25 °C (lit.)

functional group

aldehyde
fluoro

Quality Level

100

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Application

3,4-Difluorobenzaldehyde was used in the synthesis of 3-benzylidene 20,29-dihydrobetulinic acid derivatives.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

156.2 °F - DIN 51758

flash_point_c

69 °C - DIN 51758

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3133
STBD0973V
S69271V
S69271
02321EH

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Rama Mukherjee et al.
Bioorganic & medicinal chemistry letters, 14(12), 3169-3172 (2004-05-20)
New 3-O-acyl, 3-benzylidene, 3-hydrazone, 3-hydrazine, 17-carboxyacryloyl ester derivatives of betulinic acid (2-6, 8-11, 13, 17, 18, 21, and 22) were synthesized and evaluated in vitro for anti-angiogenic activity on endothelial cell cytotoxicity, specificity, and tube-formation ability. All derivatives reported here

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