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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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Chemical Structure| 1550-35-2 Chemical Structure| 1550-35-2
Chemical Structure| 1550-35-2

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Product Details of 2,4-Difluorobenzaldehyde

CAS No. :1550-35-2
Formula : C7H4F2O
M.W : 142.10
SMILES Code : O=CC1=CC=C(F)C=C1F
MDL No. :MFCD00010326
InChI Key :WCGPCBACLBHDCI-UHFFFAOYSA-N
Pubchem ID :73770

Safety of 2,4-Difluorobenzaldehyde

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H226-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338
Class:3
UN#:1989
Packing Group:

Application In Synthesis of 2,4-Difluorobenzaldehyde

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 1550-35-2 ]
  • Downstream synthetic route of [ 1550-35-2 ]

[ 1550-35-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 1550-35-2 ]
  • [ 247564-66-5 ]
References: [1] Canadian Journal of Chemistry, 2007, vol. 85, # 4, p. 283 - 292.
 

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• Alkyl Halide Occurrence • Arndt-Eistert Homologation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hunsdiecker-Borodin Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Preparation of Carboxylic Acids • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Carboxylic Acids • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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