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Chemical Structure| 1357362-21-0 Chemical Structure| 1357362-21-0

Structure of 1357362-21-0

Chemical Structure| 1357362-21-0

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Product Details of [ 1357362-21-0 ]

CAS No. :1357362-21-0
Formula : C14H12N2O
M.W : 224.26
SMILES Code : CC1=CC(N(C2=CC3=CC=CC=C3C=C2)N1)=O

Safety of [ 1357362-21-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1357362-21-0 ]

* 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 [ 1357362-21-0 ]

[ 1357362-21-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6290-17-1 ]
  • [ 2243-58-5 ]
  • [ 1192140-15-0 ]
  • [ 1357362-21-0 ]
YieldReaction ConditionsOperation in experiment
Example 26 (Comparative): Adaptation of the process by Ueda et al. 1982 for the preparation of the compound of formula (VII)/(VIIa) 5-methyl-l-(naphthalen-2-yl)-lH- pyrazol-3-olNaphthalen-2-ylhydrazine hydrochloride (30 g) and NaOMe (20,85 g) were slurried in toluene (300 ml) and heated to 80/85 °C. Ethyl 2-(2,4-dimethyl-l,3-dioxolan-2- yl)acetate (30,6 ml) was added and maintained for 90 min. Ethyl 2-(2,4-dimethyl-l,3- dioxolan-2-yl)acetate (8,2 ml) and NaOMe (2,5 g) were added and maintained for 2 h. NaOMe (1,7 g) was added and maintained for 1 h. The mixture was cooled to room temperature, water (450 ml) was added and pH adjusted to 6-8 with aqueous HC1. The organic layer was concentrated to dryness under vacuum and methanol (450 ml), HC1 35percent (18 ml) and water (54 ml) were added. The mixture was heated to reflux for 90 min and concentrated under vacuum to 165 ml of final volume. Water (120 ml) and CH2C12 (120 ml) were added and pH adjusted to 12,2-12,7 (basified with NaOH 25percent). Upper organic layer was discarded, and pH of lower aqueous layer was adjusted to 5,0- 7,0 with acetic acid 80percent. The solid was filtered, washed with water (45 ml) and slurried in ethyl acetate (102 ml) 2 h at 20/25 °C. The solid was filtered, washed with ethyl acetate (15 ml) and dried to yield 20,24 g (46percent) of a mixture [5-methyl-l- (naphthalen-2-yl)-lH-pyrazol-3-ol]: [3-methyl-l-(naphthalen-2-yl)-lH-pyrazol-5-ol] (80:20).
Example 26Adaptation of the process by Ueda et al.1982 for the preparation of 5-methyl-1-(naphthalen-2-yl)-1H -pyrazol-3-olNaphthalen-2-ylhydrazine hydrochloride (30 g) and NaOMe (20,85 g) were slurried in toluene (300 ml) and heated to 80/85 °C. Ethyl 2-(2,4-dimethyl-1,3-dioxolan-2-yl)acetate (30,6 ml) was added and maintained for 90 min.Ethyl 2-(2,4-dimethyl-1,3-dioxolan-2-yl)acetate (8,2 ml) and NaOMe (2,5 g) were added and maintained for 2 h. NaOMe (1,7 g) was added and maintained for 1 h.The mixture was cooled to room temperature, water (450 ml) was added and pH adjusted to 6-8 with aqueous HCl.The organic layer was concentrated to dryness under vacuum and methanol (450 ml), HCl 35percent (18 ml) and water (54 ml) were added.The mixture was heated to reflux for 90 min and concentrated under vacuum to 165 ml of final volume.Water (120 ml) and CH2Cl2 (120 ml) were added and pH adjusted to 12,2-12,7 (basified with NaOH 25percent).Upper organic layer was discarded, and pH of lower aqueous layer was adjusted to 5,0-7,0 with acetic acid 80percent.The solid was filtered, washed with water (45 ml) and slurried in ethyl acetate (102 ml) 2 h at 20/25 °C.The solid was filtered, washed with ethyl acetate (15 ml) and dried to yield 20,24 g (46percent) of a mixture [5-methyl-1-(naphthalen-2-yl)-1H-pyrazol-3-ol]: [3-methyl-1-(naphthalen-2-yl)-1H-pyrazol-5-ol] (80:20).
 

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