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tetraethyl 2-(4-(trifluoromethyl)phenyl)ethene-1,1-diyldiphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149589-34-4

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149589-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149589-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,8 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149589-34:
(8*1)+(7*4)+(6*9)+(5*5)+(4*8)+(3*9)+(2*3)+(1*4)=184
184 % 10 = 4
So 149589-34-4 is a valid CAS Registry Number.

149589-34-4Relevant academic research and scientific papers

Dioxirane oxidation of 2-Aryl-1-vinyl-1, 1-diphosphane dioxide: A convenient approach for the synthesis of novel 1,2-epoxy-2-aryl ethylgembisphosphonates

Fotsing, Marthe Carine Djuidje,Coville, Neil,Mbianda, Xavier Yangkou

, p. 234 - 241 (2013/07/05)

The synthesis of tetraethyl 1,2-epoxy-2-aryl ethylgembisphosphonates by direct epoxidation of 2-aryl,vinyl-1,1-diphosphonate derivatives with ethyl methyldioxirane generated in situ from potassium hydrogen monopersulfate (caroate) and butanone in a phase

A Facile Cu(I)/TF-BiphamPhos-catalyzed asymmetric approach to unnatural α-amino acid derivatives containing gem-bisphosphonates

Xue, Zhi-Yong,Li, Qing-Hua,Tao, Hai-Yan,Wang, Chun-Jiang

supporting information; experimental part, p. 11757 - 11765 (2011/09/16)

A novel catalytic asymmetric Michael addition of azomethine ylide with β-substituted alkylidene bisphosphates was realized in the presence of a chiral copper(I)/TF-BiphamPhos complex. The present system provides a unique and facile access to enantioenriched unnatural α-amino acid derivatives containing gem-bisphosphonates (gem-BPs) in high yields with excellent diastereoselectivities and enantioselectivities. Subsequent transformations lead to the expedient preparation of biologically active unnatural α-amino acid derivatives containing BPs and bisphosphonic acids without loss of diastereo- and enantiomeric excess.

Guanidinoalkyl-1,1-bisphosphonic acid derivatives, process for their preparation and their use

-

, (2008/06/13)

The invention describes tautomeric compounds of the formula Ia, Ib or Ic STR1 and/or their physiologically tolerable salts, in which R1, R2, R3, R4, R5, R6 and R7 are a hydrogen atom, substituted (C1 -C7)-alkyl, (C3 -C10)-cycloalkyl, substituted phenyl or (C1 -C4)-alkylphenyl, R2 is substituted phosphoric acid, R2 and R3, R2 and R5 or R4 and R5 form a monocyclic 5- to 7-membered saturated or unsaturated heterocyclic ring which is mono- or polysubstituted, R8, R9, R10 and R11 are a hydrogen atom or (C1 -C5)-alkyl, X is a hydrogen atom, hydroxyl or halogen, l and n are an integer from 0 to 7, m is an integer from 0 to 2, and the sum of the numbers l, m and n is less than or equal to 10, a process for the preparation of the compounds of the formula Ia, Ib or Ic, pharmaceuticals and their use for the prophylaxis or treatment of osteoporosis.

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