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(3-methyl-1-phenyl-1H-pyrazol-4-yl)-phosphonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40170-99-8

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40170-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40170-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40170-99:
(7*4)+(6*0)+(5*1)+(4*7)+(3*0)+(2*9)+(1*9)=88
88 % 10 = 8
So 40170-99-8 is a valid CAS Registry Number.

40170-99-8Downstream Products

40170-99-8Relevant academic research and scientific papers

The synthesis of phosphonyl pyrazoles

Chen, Hu,Qian, Ding-Quan,Xu, Guo-Xiang,Liu, Yu-Xiu,Chen, Xiao-Dong,Shi, Xiao-Dong,Cao, Ru-Zhen,Liu, Lun-Zu

, p. 85 - 88 (2007/10/03)

Phosphonyl hydrazones react with DMF/POCl3 to afford 3-phos-phonyl pyrazoles. Phosphonyl methylene hydrazones react with DMF/POCl3 to provide 4-phosphonyl pyrazoles. 5-phosphonyl pyrazoles are obtained from the reaction of phosphonyl chlorovinylaldchydes with phenylhydrazine.

New strategy for the synthesis of phosphonyl pyrazoles

Chen, Hu,Qian, Ding-Quan,Xu, Guo-Xiang,Liu, Yu-Xiu,Chen, Xiao-Dong,Shi, Xiao-Dong,Cao, Ru-Zhen,Liu, Lun-Zu

, p. 4025 - 4033 (2007/10/03)

Phosphonyl hydrazones react with DMF/POCl3 to afford 3-phosphonyl pyrazoles. Phosphonyl methylene hydrazones react with DMF/POCl3 to provide 4-phosphonyl pyrazoles. 5-Phosphonyl pyrazoles are obtained from the reaction of phosphonyl chlorovinylaldehydes with phenylhydrazine.

SYNTHESE D'HETEROCYCLES α-PHOSPHONIQUES. NOUVEAUX DEVELOPPEMENTS

Aboujaoude, Elie Elia,Collignon, Noel,Savignac, Philippe

, p. 231 - 244 (2007/10/02)

Synthesis of α-phosphonic heterocycles is described by condensation of 1,2- 1,3- or 1,4-bisnucleophiles with β-phosphonic enamines 2 bearing a functional group.From guanidine and analogs 4-diethoxyphosphinyl pyrimidines 5 and 8 are obtained with yields up to 50percent .Substituted hydrazines give 4-diethoxyphosphinyl pyrazoles 11 with very good yields.With hydroxylamine a spontaneous dehydration gives the enolic form 18 of a β-ketophosphonate α-nitrile.Orthophenylene diamine is a special example in fact the departure β-ketophosphonate is recovered with benzimidazole elimination.

DIALKYL FORMYL-1 METHYLPHOSPHONATES α-FONCTIONNELS-II. PREPARATION PAR VOIE THERMIQUE ET TRANSFORMATION EN HETEROCYCLES α-PHOSPHONIQUES

Aboujaoude, Elie Elia,Collignon, Noel,Savignac, Philippe

, p. 427 - 434 (2007/10/02)

The thermal condensation of functional phosphonates bearing strongly withdrawing groups (RO)2P(O)CH2Z 1 with dimethylformamide dimethyl acetal gives corresponding β-functional, β-phosphonic enamines (RO)2P(O)C(Z)=CHNMe2 2.Acid or basic hydrolysis of the enamines frequently gives the free aldehyde (RO)2P(O)CH(Z)-CHO 3.We show that the enamines can be used with success for the synthesis of heterocycles like, pyrazoles 4, pyrimidines 5, benzodiazepine 6 or indole 7, all of them substituted with a phosphonate group.

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