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Chemistry
Organic Building Blocks
Aryls
2-Chloro-N-(4-(diethylamino)phenyl)acetamide
Chemistry
Organic Building Blocks
Aryls
Amines Chlorides Amides

[ CAS No. 125983-31-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 125983-31-5
Chemical Structure| 125983-31-5
Structure of 125983-31-5 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 125983-31-5 ]

COA NMR CNMR HPLC LC-MS

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SDS Specification
Alternatived Products of [ 125983-31-5 ]

Product Details of [ 125983-31-5 ]

CAS No. :125983-31-5 MDL No. :MFCD00791331
Formula : C12H17ClN2O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 240.73 Pubchem ID :-
Synonyms :

Safety of [ 125983-31-5 ]

Signal Word: Class:
Precautionary Statements: UN#:
Hazard Statements: Packing Group:

Application In Synthesis of [ 125983-31-5 ]

* 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 [ 125983-31-5 ]

[ 125983-31-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 79-04-9 ]
  • [ 93-05-0 ]
  • [ 125983-31-5 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; benzene
With acetic acid
Reference： [1]Jacobs; Heidelberger [Journal of Biological Chemistry, 1915, vol. 21, p. 150]
[2]Location in patent: experimental part Stamatoiu, Oana; Bubnov, Alexej; Ţârcomnicu, Isabela; Iovu, Mircea [Journal of Molecular Structure, 2008, vol. 886, # 1-3, p. 187 - 196]
  • 2
  • [ 125983-31-5 ]
  • [ 74-88-4 ]
  • [ 125983-12-2 ]
YieldReaction ConditionsOperation in experiment
With sulfur; triethylamine 1.) DMF, 2 h, 2.) 10 deg C, H2O; Yield given. Multistep reaction;
Reference： [1]Thiel, W.; Mayer, R. [Journal fur praktische Chemie (Leipzig 1954), 1989, vol. 331, # 2, p. 243 - 262]
  • 3
  • [ 125983-31-5 ]
  • [ 2227-79-4 ]
  • <i>N</i>,<i>N</i>-diethyl-<i>N</i>'-(2-phenyl-thiazol-4-yl)-benzene-1,4-diamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
In N,N-dimethyl-formamide at 80℃; for 12h;
Reference： [1]Warashina, Masaki; Kyung, Hoon Min; Kuwabara, Tomoko; Huynh, Alexis; Gage, Fred H.; Schultz, Peter G.; Ding, Sheng [Angewandte Chemie - International Edition, 2006, vol. 45, # 4, p. 591 - 593]
  • 4
  • [ 125983-31-5 ]
  • <i>N</i>,<i>N</i>-diethyl-<i>N</i>'-methyl-<i>N</i>'-(2-phenyl-thiazol-4-yl)-benzene-1,4-diamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: dimethylformamide / 12 h / 80 °C 2: NaH / tetrahydrofuran / 2 h / 20 °C
Reference： [1]Warashina, Masaki; Kyung, Hoon Min; Kuwabara, Tomoko; Huynh, Alexis; Gage, Fred H.; Schultz, Peter G.; Ding, Sheng [Angewandte Chemie - International Edition, 2006, vol. 45, # 4, p. 591 - 593]
  • 5
  • 4-[(4-methoxybenzylidene)amino]phenol [ No CAS ]
  • [ 125983-31-5 ]
  • C26H29N3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
38.21% Stage #1: 4-[(4-methoxybenzylidene)amino]phenol With sodium hydroxide In ethanol; benzene for 0.666667h; Reflux; Stage #2: chloro-acetic acid-(4-diethylamino-anilide) In ethanol; benzene for 10h; Reflux;
Reference： [1]Location in patent: experimental part Stamatoiu, Oana; Bubnov, Alexej; Ţârcomnicu, Isabela; Iovu, Mircea [Journal of Molecular Structure, 2008, vol. 886, # 1-3, p. 187 - 196]

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