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Chemical Structure| 112966-26-4 Chemical Structure| 112966-26-4

Structure of 112966-26-4

Chemical Structure| 112966-26-4

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Product Details of [ 112966-26-4 ]

CAS No. :112966-26-4
Formula : C12H10ClNO
M.W : 219.67
SMILES Code : O[C@H](C1=CC=C(Cl)C=C1)C2=NC=CC=C2

Safety of [ 112966-26-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 112966-26-4 ]

* 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 [ 112966-26-4 ]

[ 112966-26-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 17624-36-1 ]
  • [ 104-88-1 ]
  • [ 176022-47-2 ]
  • [ 112966-26-4 ]
  • 2
  • [ 6318-51-0 ]
  • [ 176022-47-2 ]
  • [ 112966-26-4 ]
YieldReaction ConditionsOperation in experiment
With Kluyveromyces polysporus alcohol dehydrogenase S237R mutant; isopropyl alcohol; NADPH; In aq. phosphate buffer; at 30℃;pH 7.0;Enzymatic reaction;Kinetics; Catalytic behavior; General procedure: Bioconversion was conducted with 20 mM 1a-10a,20 U·mL-1KpADH variants, 40 mM isopropanol in PBS buffer (pH 7.0,100 mM) in total volume of 2 mL at 30 C and 180 rpm overnight. Then,1 mL of the reaction mixture was withdrawn and extracted with ethylacetate. The organic phase was isolated by centrifugation and driedover anhydrous MgSO4. The conversion rate and enantioselectivity ofthe products were analyzed as described in supporting information.
With Kluyveromyces polysporus alcohol dehydrogenase E214 G/S237C mutant variant; NADPH; In aq. phosphate buffer; at 30℃;pH 7.0;Enzymatic reaction;Kinetics; General procedure: Six variants with significantly improved activity were selected to test their stereoselectivity and conversion rate. Bioconversion was conducted with 20mM 1a-9a, 20UmL-1 KpADH or variants in PBS buffer (pH 7.0, 100mM) in total volume of 2mL at 30C and 180rpm overnight. Then, 1mL of the reaction mixture was withdrawn and extracted with equal volume of ethyl acetate. The organic phase was isolated by centrifugation at 12000×g for 2min, and dried over anhydrous MgSO4. The conversion rate and stereoselectivity of the products were determined using the Agilent 1100 equipped with a Chiralcel OB-H column or a Chiralcel OD-H column (0.46mm×250mm×5μm, Diacel, Japan). Detailed conditions for stereoselectivity analysis and the retention times of (R)- and (S)-alcohols could be found in Table S3 [28].
  • 3
  • [ 27652-89-7 ]
  • [ 176022-47-2 ]
  • [ 112966-26-4 ]
  • 4
  • C32H21BClNO3 [ No CAS ]
  • [ 176022-47-2 ]
  • [ 112966-26-4 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In ethyl acetate; at 20℃; for 1h; General procedure: (Step 2) Spiroborate complex (200 mg, 0.389 mmol) was partitioned between ethyl acetate (30 ml) and 2N hydrochloric acid (20 ml) and stirred at room temperature for 1 hour.After washing the separated aqueous layer with ethyl acetate (10 ml) and adjusting the pH to 7 with saturated sodium hydrogen carbonate,Extracted with dichloromethane (2 x 20 ml).The extracted organic layers were combined, dried over anhydrous sodium sulfate and concentrated to give compound 1 (84 mg, 0.38 mmol, 98% ee).
 

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