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2,6-diiodo-3,5-dimethyoxyphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147622-60-4

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147622-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147622-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147622-60:
(8*1)+(7*4)+(6*7)+(5*6)+(4*2)+(3*2)+(2*6)+(1*0)=134
134 % 10 = 4
So 147622-60-4 is a valid CAS Registry Number.

147622-60-4Relevant academic research and scientific papers

Synthesis of 4,7,9-Trihydroxy[1]benzofuro[3,2-d]pyrimidine-6-carboxamide: Evaluation of Cytotoxicity and Inhibition of Protein Kinase C (Ca Pkc1)

Hung, Dao Viet,Vu, Tran Khac

, (2021/08/12)

The protein kinase Pkc1 of Candida albicans (CaPkc1), one of the key proteins involved in MAPK pathway, is described as a regulator of cell wall integrity during growth, morphogenesis, and response to cell wall stress. The (-)-cercosporamide is an antifun

Iodine(III)-Mediated, Controlled Di- or Monoiodination of Phenols

Satkar, Yuvraj,Yera-Ledesma, Luisa F.,Mali, Narendra,Patil, Dipak,Segura-Quezada, Luis A.,Ramírez-Morales, Perla I.,Solorio-Alvarado, César R.,Navarro-Santos, Pedro

, p. 4149 - 4164 (2019/04/30)

An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylbenzene as a nontoxic iodine(III)-based oxidant and ammonium iodide as a cheap iodine atom source. A totally controlled monoiodination was achieved by buffering the reaction medium with K3PO4. This protocol proceeds with short reaction times, at mild temperatures, in an open flask, and generally with high yields. Gram-scale reactions, as well as the scope of this protocol, were explored with electron-rich and electron-poor phenols as well as heterocycles. Quantum chemistry calculations revealed PhII(OH)·NH3 to be the most plausible iodinating active species as a reactive "I+" synthon. In light of the relevance of the iodoarene moiety, we present herein a practical, efficient, and simple procedure with a broad functional group scope that allows access to the iodoarene core unit.

Elaboration of simplified vinca alkaloids and phomopsin hybrids

Ngo, Quoc Anh,Roussi, Fanny,Thoret, Sylviane,Gueritte, Francoise

experimental part, p. 284 - 294 (2010/12/19)

Nine simplified vinca alkaloids and phomospin A hybrids, in which vindoline moiety has been replaced by a simpler scaffold, have been elaborated to evaluate their activity on the inhibition of tubulin polymerization. This article deals with the synthesis of various simplified vinca alkaloids, using a stereoselective coupling of catharantine with reactive aromatic compounds and methanol as well as their subsequent condensation with a large peptide chain mimicking those of phomopsin A. Biological evaluation and molecular modeling studies are also reported.

Synthesis of halogenated phenols by directed ortho-lithiation and ipso-iododesilylation reactions of O-aryl N-isopropylcarbamates

Kauch, Matthias,Hoppe, Dieter

, p. 1578 - 1589 (2007/10/03)

The regioselective synthesis of halogenated phenols via directed ortho-lithiation reactions of in situ N-silylated O-aryl N-isopropylcarbamates is reported. This protocol is complemented by ipso-iododesilylation reactions of C-silylated carbamates and iodine-magnesium exchange reactions, which are facilitated by the adjacent carbamoyl group. These methods provide an entry into a series of o-fluoro-, o-iodo-, and o,o′-diiodophenols in high yields which are otherwise difficult to obtain. Georg Thieme Verlag Stuttgart.

A Formal Synthesis of Aflatoxin B2

Weeratunga, Gamini,Horne, Stephen,Rodrigo, Russell

, p. 721 - 722 (2007/10/02)

A brief synthesis of a ring A differentiated tetrahydrofurobenzofuran intermediate previously converted into Aflatoxin B2 is described.

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