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Chemical Structure| 21254-22-8 Chemical Structure| 21254-22-8

Structure of 21254-22-8

Chemical Structure| 21254-22-8

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Product Details of [ 21254-22-8 ]

CAS No. :21254-22-8
Formula : C8H8Cl2N4
M.W : 231.08
SMILES Code : CC(N1N=CC2=C(Cl)N=C(Cl)N=C21)C
MDL No. :MFCD12405952
InChI Key :SHTPXXJWYCEZPN-UHFFFAOYSA-N
Pubchem ID :42609352

Safety of [ 21254-22-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 21254-22-8 ]

* 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 [ 21254-22-8 ]

[ 21254-22-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 21254-22-8 ]
  • [ 15996-84-6 ]
  • 6-chloro-1-(1-methylethyl)-N-{1-[4-(trifluoromethyl)phenyl]ethyl}-1H-pyrazolo[3,4-d]pyrimidin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; at 50℃; A solution of 4,6-dichloro-1-isopropyl-1H-pyrazolo[3,4-djpyrimidine (54 mg, 0.234 mmol) and TEA(100 tL, 0.72 mmol) in 1 mL THF was prepared. 1-[4-(Trifluoromethyl)phenyljethan-1-amine (88mg, 0.468 mmol) was then added to the reaction mixture and it was stirred overnight at 50 C on aheating block. The next day, the reaction mixture was transferred to a l3xlOOmm test tube, and theTHF was removed under a stream of nitrogen. The crude residue was then dissolved in DMSO (1 mL)and purified by mass-directed HPLC (2 cm x 5cm C18, acetonitrile-water gradient, 0.05% NH4OHadded) to afford the product as a solid. LC-MS (+ESI) m/z = 384.4 and 386.3 (M+2+H)t
 

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Related Functional Groups of
[ 21254-22-8 ]

Chlorides

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Related Parent Nucleus of
[ 21254-22-8 ]

Other Aromatic Heterocycles

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