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cis-2-phenyltetrahydropyran-6-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124469-06-3

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124469-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124469-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124469-06:
(8*1)+(7*2)+(6*4)+(5*4)+(4*6)+(3*9)+(2*0)+(1*6)=123
123 % 10 = 3
So 124469-06-3 is a valid CAS Registry Number.

124469-06-3Downstream Products

124469-06-3Relevant academic research and scientific papers

NEW CCR2 RECEPTOR ANTAGONISTS AND USES THEREOF

-

Page/Page column 50, (2012/01/14)

The present invention relates to novel antagonists for CCR2 (CC chemokine receptor 2) and their use for providing medicaments for treating conditions and diseases, especially pulmonary diseases like asthma and COPD.

Masked Lithium Bishomoenolates: Useful Intermediates in Organic Synthesis

Ramon, Diego J.,Yus, Miguel

, p. 3825 - 3831 (2007/10/02)

The lithiation of the chloro ketals 9 with lithium naphthalenide at -78 deg C led to the corresponding masked lithium bishomoenolates 4, which are stable species under these conditions and react with different electrophilic reagents (H2O, D2O, i-PrCOH, Ph

Stereoselective Syntheses of α-Substituted Cyclic Ethers and syn-1,3-Diols

Homma, Koichi,Takenoshita, Haruhiro,Mukaiyama, Teruaki

, p. 1898 - 1915 (2007/10/02)

In the presence of a catalytic amount of triphenylmethylium hexachloroantimonate or a catalyst system of antimony pentachloride, chlorotrimethylsilane and tin(II)iodide, α-substituted cyclic ethers are stereoselectively prepared from lactones by successiv

SUBSTITUTION REACTIONS OF 2-BENZENESULPHONYL CYCLIC ETHERS WITH CARBON NUCLEOPHILES

Brown, Dearg S.,Bruno, Maurizio,Davenport, Raymond J.,Ley, Steven V.

, p. 4293 - 4308 (2007/10/02)

Direct substitution of 2-benzenesulphonylcyclic ethers was studied using a variety of carbon nucleophiles.These nucleophiles included organozinc reagents (derived from aryl, vinyl and alkynyl Grignard reagents) or silyl enol ethers, silyl ketene acetals,

SUBSTITUTION REACTIONS OF 2-BENZENESULPHONYL CYCLIC ETHERS WITH SILYL ENOL ETHERS PROMOTED BY ALUMINIUM TRICHLORIDE

Brown, Dearg S.,Ley, Steven V.,Bruno, Maurizio

, p. 773 - 777 (2007/10/02)

Several cyclic ether 2-benzenesulphones were shown to react with silyl enol ethers in the presence of AlCl3 to give the corresponding alkylated products in good yield.Where substitution occured to give 2,6-disubstituted products there was a marked prefere

A CONVENIENT SYNTHESIS OF CYCLIC ETHERS FROM SILOXY CARBONYL COMPOUNDS

Homma, Koichi,Mukaiyama, Teruaki

, p. 259 - 262 (2007/10/02)

Five-seven membered cyclic ethers are prepared by one-pot procedure in good yields from γ-, δ-, and ε-siloxy carbonyl compounds, respectively, on treatment with silyl nucleophiles (triethylsilane, allyltrimethylsilane, trimethylsilyl cyanide, etc.) in the

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