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Chemical Structure| 41373-37-9 Chemical Structure| 41373-37-9

Structure of 41373-37-9

Chemical Structure| 41373-37-9

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Product Details of [ 41373-37-9 ]

CAS No. :41373-37-9
Formula : C13H10N2O
M.W : 210.23
SMILES Code : NC1=CC=C(OC(C2=CC=CC=C2)=N3)C3=C1
MDL No. :MFCD00453044
InChI Key :SUOXXPHZWVBJSY-UHFFFAOYSA-N
Pubchem ID :721059

Safety of [ 41373-37-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P264-P270-P280-P301+P312+P330-P305+P351+P338-P337+P313-P501

Application In Synthesis of [ 41373-37-9 ]

* 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 [ 41373-37-9 ]

[ 41373-37-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 41373-37-9 ]
  • [ 42860-10-6 ]
  • 3-bromo-4-chloro-N-(2-phenylbenzo[d]oxazol-5-yl)benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% General procedure: Substituted benzoic acid or substituted phenylacetic acid 4(1 mmol) was added to a 50-mL round bottom flask and dissolvedwith DMF (20 mL), HOBt (1.5 mmol), EDCI (1.5 mmol), and TEA(1.5 mmol). Then, the solution was stirred at room temperature for10 min. DMF was added to dissolve 2-phenyl benzoxazole structure3, and then the solution was continuously stirred for 2e4 h. Thereaction was monitored by TLC and then stopped after completionwas indicated. The resultant solution was extracted with ethyl acetate(15 mL), washed twice with dilute hydrochloric acid (50 mL),and the organic phase was dried over anhydrous sodium sulfateand separated by silica gel column chromatography (petroleumether: ethyl acetate 2: 1). A yellow or white solid product 5 wasobtained (yield > 85%).
1 mmol of substituted benzoic acid or substituted phenylacetic acid 4 was added to a 20 mL round bottom flask and dissolved in 20 mL of DMF. 1.5 mmol of HOBT, 1.5 mmol of EDCI and 2 mmol of TEA triethylamine were added successively and then treated with a normal temperature magnetic stirrer Stirring about 10min,And then added with DMF dissolved in 2-phenyl benzoxazole 3, stirring at room temperature, reaction 2-4h, TLC detection of raw materials reaction is completed, stop stirring, add ethyl acetate 15mL extraction, and then dilute hydrochloric acid 50mL wash 2 times, The organic phase was dried over anhydrous sodium sulfate for 30 min and isolated by silica gel column chromatography (petroleum ether: ethyl acetate = 2: 1) to give the product 5-3 as a yellowish white solid product.
  • 2
  • [ 41373-37-9 ]
  • [ 97-08-5 ]
  • 4-chloro-3-nitro-N-(2-phenylbenzo[d]oxazol-5-yl)benzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine; In dichloromethane; at 20℃; for 18h; General procedure: To stirring mixtures of either 4-(1,3-benzoxazol-2-yl)aniline or 2-phenyl-1,3-bezoxazol-5-amine (1 eq.) in anhydrous CH2Cl2 (5 mL) were added the respective R1-sulfonyl chlorides (1.3 eq.), followed by anhydrous pyridine (1.3 eq.). The reactions were allowed to stir at room temperature for 18 h, then chromatographed over silica (hexanes:EtOAc gradient), and concentrated. If necessary, the products were further purified by preparatory RP-HPLC (H2O:CH3CN gradient), concentrated, and lyophilized. Refer below for individual compound characterization data.
 

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