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4-(2-amino-4-methylphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158461-63-3

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158461-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158461-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,4,6 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 158461-63:
(8*1)+(7*5)+(6*8)+(5*4)+(4*6)+(3*1)+(2*6)+(1*3)=153
153 % 10 = 3
So 158461-63-3 is a valid CAS Registry Number.

158461-63-3Relevant academic research and scientific papers

RhII2-catalyzed synthesis of α-, β-, or δ-carbolines from aryl azides

Pumphrey, Ashley L.,Dong, Huijun,Driver, Tom G.

supporting information; experimental part, p. 5920 - 5923 (2012/08/07)

Approaching all isomers: A range of α-, β- and δ-carbolinium ions are readily available from ortho-substituted aryl azides using a rhodium(II) carboxylate catalyst (see scheme). The carbolinium ions are readily reduced to afford tryptolines or deprotonated to access pyridoindoles. This [RhII2]-catalyzed C-H bond amination was used in the synthesis of (±)-horsfiline and neocryptolepine. esp=α,α,α',α'- tetramethyl-1,3-benzenedipropionate. Copyright

COMPOUNDS USEFUL FOR INHIBITING CHK1

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Page/Page column 44, (2008/06/13)

Substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as ther-apeutic agents, for example, in treating cancer and oth

Synthesis and antiarrhythmic activity of disubstituted phenylpyridine derivative

Shigyo,Sato,Shibuya,Takahashi,Yamaguchi,Sonoki,Ohta

, p. 1573 - 1582 (2007/10/02)

A series of disubstituted phenylpyridine derivatives was synthesized and their antiarrhythmic effects against chloroform-induced ventricular arrhythmias in mice were examined. Among them, 2- and 3-[2-(3- aminobutyramido)-4-(2,2,2-trifluoroethoxy)phenyl]pyridines (23h, 24h) and 3- [2-(3-aminobutyramido)-4-ethoxyphenyl]pyridine (24i) showed potent antiarrhythmic activity. They had approximately twice the potency of mexiletine (III). Compound 24i was selected from this series as a candidate for further development; it was found to have a class I B electrophysiological character and to show a slow kinetic rate-dependent block (RDB) of the sodium channel in cardiac muscle.

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