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Chemical Structure| 6470-87-7 Chemical Structure| 6470-87-7

Structure of 6470-87-7

Chemical Structure| 6470-87-7

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Product Details of [ 6470-87-7 ]

CAS No. :6470-87-7
Formula : C15H7ClO3
M.W : 270.67
SMILES Code : O=C(Cl)C(C=C1C2=O)=CC=C1C(C3=C2C=CC=C3)=O
MDL No. :MFCD00059498
InChI Key :DGJNWQJOASAMHY-UHFFFAOYSA-N
Pubchem ID :15025286

Safety of [ 6470-87-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H290-H314
Precautionary Statements:P234-P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P390-P405-P406-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 6470-87-7 ]

* 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.

  • Downstream synthetic route of [ 6470-87-7 ]

[ 6470-87-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 117-78-2 ]
  • [ 6470-87-7 ]
YieldReaction ConditionsOperation in experiment
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 2h;Inert atmosphere; This example and the following Examples 2 and 3 describe compounds and methods of the invention for making an ASM-amide-linked sol-gel matrix material and corresponding WE of the invention. Anthraquinone-2-carboxylic acid (0.500 g, 1.98 mmol) was suspended in dichloromethane (20 mL) in a vial, and then the vial was purged with nitrogen. 0.2 mL of dimethylformamide (DMF) was added dropwise, followed by addition of oxalyl chloride (0.18 mL, 2.2 mmol). The solution was stirred for 2 h. Then, diethylaminomethylpolystyrene (1.97 g, 6.3 mmol of amine) was added followed by 3-aminopropyltrimethoxysilane (APTOS) (0.37 mL, 2.1 mmol). Stirring was continued for 16 h at ambient temperature. The resultant liquid was filtered to remove the diethylaminomethylpolystyrene solid. Additional dichloromethane was used to rinse the retained solid to recover entrained product. The dichloromethane was removed in a rotary evaporator to obtain an amber oily liquid. Anhydrous alcohol was used to reconstitute the oily liquid to obtain 20 mL of the amide-linked AQ silane solution.
With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane;Reflux; 9,10-<strong>[117-78-2]anthraquinone-2-carboxylic acid</strong> (1.86 g, 7.4 mmol) was added to a 100 mL reaction flask,Thionyl chloride (1.05 g, 8.9 mmol), dichloromethane (30 mL), catalytic amount of DMF, reflux reaction overnight, to be completely clear solution to be -9,10-anthraquinone-2-formyl chloride in dichloromethane solution, Directly for the next step
References: [1]European Journal of Medicinal Chemistry,2007,vol. 42,p. 752 - 771.
[2]Journal of Organic Chemistry,1992,vol. 57,p. 6143 - 6150.
[3]Chemistry - A European Journal,2002,vol. 8,p. 5630 - 5643.
[4]Journal of the American Chemical Society,1994,vol. 116,p. 9847 - 9859.
[5]Journal of the Indian Chemical Society,1932,vol. 9,p. 375.
[6]Bulletin of the Chemical Society of Japan,1932,vol. 7,p. 114,117, 118.
[7]Chemische Berichte,1884,vol. 17,p. 890.
[8]Helvetica Chimica Acta,1926,vol. 9,p. 802.
[9]Liebigs Annalen der Chemie,1981,p. 792 - 810.
[10]Journal of Medicinal Chemistry,1982,vol. 25,p. 369 - 373.
[11]Journal of the American Chemical Society,1989,vol. 111,p. 5542 - 5551.
[12]Helvetica Chimica Acta,1980,vol. 63,p. 413 - 419.
[13]Journal of Organic Chemistry,1996,vol. 61,p. 1297 - 1301.
[14]Journal of Physical Chemistry A,2000,vol. 104,p. 8315 - 8322.
[15]Bulletin of the Chemical Society of Japan,2000,vol. 73,p. 2051 - 2058.
[16]Organic letters,2000,vol. 2,p. 3413 - 3416.
[17]Journal of Organic Chemistry,2000,vol. 65,p. 5355 - 5359.
[18]Chemical Communications,2009,p. 5281 - 5283.
[19]European Journal of Inorganic Chemistry,2014,vol. 2014,p. 1984 - 2001.
[20]Patent: US9417204,2016,B2 .Location in patent: Page/Page column 24; 25.
[21]Patent: CN104788333,2017,B .Location in patent: Paragraph 0189-0191.
[22]Chemical Biology and Drug Design,2018,vol. 91,p. 893 - 901.
[23]Chemical Communications,2018,vol. 54,p. 3038 - 3041.
[24]Angewandte Chemie - International Edition,2018,vol. 57,p. 16871 - 16876.
    Angew. Chem.,2018,vol. 130,p. 17113 - 17118,6.
  • 2
  • [ 1454-85-9 ]
  • [ 6470-87-7 ]
  • [ 143657-42-5 ]
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • General Reactivity • Grignard Reaction • Heat of Combustion • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reformatsky Reaction • Robinson Annulation • Rosenmund Reduction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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