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[ CAS No. 31867-92-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 31867-92-2
Chemical Structure| 31867-92-2
Structure of 31867-92-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 31867-92-2 ]

CAS No. :31867-92-2 MDL No. :MFCD18258906
Formula : C10H9ClN2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 192.64 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 31867-92-2 ]

* 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 [ 31867-92-2 ]

[ 31867-92-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 52537-00-5 ]
  • [ 31867-92-2 ]
  • 4-(6-Chloro-2,3-dihydro-indol-1-yl)-6,7-dimethyl-quinazoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
16% Example 95 4-(6-Chloro-2,3-dihydro-indol-1-yl)-6,7-dimethyl-quinazoline Utilizing a procedure analogous to that described in Example 24, this product was prepared in 16% yield from <strong>[52537-00-5]6-chloro-indoline</strong> and 4-chloro-6,7-dimethyl-quinazoline. (M.P. 199 C.; LC-MS: 310 (MH+)).
  • 2
  • [ 2243-47-2 ]
  • [ 31867-92-2 ]
  • (6,7-dimethylquinazolin-4-yl)-(biphenyl-3'-yl)amine hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; General procedure for 4-anilinoquinazolines 5-18, 34-36 General procedure: A mixture of 4-chloroquinazoline (23a-c,[1] 23d-f, 31-33[3]) (0.5 mmol) and the appropriate aniline (0.5 mmol) in i-PrOH (1 mL) was microwave irradiated at 80 °C (power set point 60 W; ramp time1 min; hold time 15 min). After cooling, the obtained precipitate was collected by filtration to give compounds 5-18 and 33-35 as hydrochlorides.
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