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1-[(1-(2-chloro-phenyl))-(5- methyl-isoxazol-3-ylamino)-methyl]-naphthalen-2- ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119485-32-4

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119485-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119485-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,8 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119485-32:
(8*1)+(7*1)+(6*9)+(5*4)+(4*8)+(3*5)+(2*3)+(1*2)=144
144 % 10 = 4
So 119485-32-4 is a valid CAS Registry Number.

119485-32-4Relevant academic research and scientific papers

Synthesis of 3-aminoisoxazolmethylnaphthols via one-pot three-component reaction under solvent-free conditions

Safarzaei, Mohyeddin,Maghsoodlou, Malek Taher,Mollashahi, Ebrahim,Hazeri, Nourallah,Lashkari, Mojtaba

, p. 7449 - 7458 (2018)

A one-pot three-component condensation reaction of 3-amino-5-methylisoxazole, aryl aldehyde and 2-naphthol to afford the corresponding 3-amino isoxazolmethylnaphthols in good to excellent yields. The remarkable features of this new procedure are high conv

Synthesis and characterization of a novel and reusable Fe3O4@THAM-CH2CH2-SCH2CO2H magnetic nanocatalyst for highly efficient preparation of xanthenes and 3-aminoisoxazoles in green conditio

Rezaie Kahkhaie, Mahboobeh,Hazeri, Nourallah,Maghsoodlou, Malek Taher,Yazdani-Elah-Abadi, Afshin

, p. 5007 - 5025 (2021/08/13)

In the present study, the synthesis and catalytic application of a novel thioglycolic acid doped on Fe3O4 nanomagnetic particles coated with tris(hydroxymethyl)aminomethane (THAM) and 1,2-dichloroethane are described. The morphology,

Synthesis of 1,3-Diaryl-2-(5-methyl-3-isoxazolyl)-2,3-dihydro-1H-naphthoxazines

Rao, E. Thirmal,Rajanarendar, E.,Krishnamurthy, A.

, p. 686 - 688 (2007/10/02)

Interaction of 3-benzalamino-5-methylisoxazoles (1) with β-naphthol in acetic acid affords the open chain α-aminomethyl-β-naphthols (2) instead of the expected 1,3-naphthoxazines (3).Treatment of 2 with 1 in acetic acid in the presence of traces of conc.H2SO4 gives the oxazines (3).

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