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5-(Hydroxyphenylmethyl)-1-methylimidazol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24132-86-3

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24132-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24132-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24132-86:
(7*2)+(6*4)+(5*1)+(4*3)+(3*2)+(2*8)+(1*6)=83
83 % 10 = 3
So 24132-86-3 is a valid CAS Registry Number.

24132-86-3Downstream Products

24132-86-3Relevant academic research and scientific papers

Substituted phenyl farnesyltransferase inhibitors

-

, (2012/09/25)

Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhibit farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.

Synthesis and application of imidazole derivatives. Introduction of carbogenic substituents into the 5-position of 1-methyl-1H-imidazole

Ohta,Yamamoto,Kawasaki,Yamashita,Katsuma,Nasako,Kobayashi,Ogawa

, p. 2681 - 2685 (2007/10/02)

The 5-position of 1-methyl-2-phenylthio-1H-imidazole (12a) was lithiated by lithium 2,2,6,6-tetramethylpiperidide, and the produced carbanion was reacted with various electrophiles to give the corresponding 5-substituted derivatives in good yields. The re

Carbodesilylation of (Trimethylsilyl)imidazoles and -pyrazoles

Effenberger, Franz,Roos, Michael,Ahmad, Roshan,Krebs, Andreas

, p. 1639 - 1650 (2007/10/02)

The preparation of the 1-methyl(trimethylsilyl) (TMS)-substituted imidazoles 3a, 4a, 8, 9, and 11a by silylation of the corresponding metallated imidazoles is described.Carbodesilylation of 3 with aldehydes or carboxylic halogenides occurs selectively in 2-position.In the presence of a strong base (CsF) the reactivity against carbon electrophiles correlates well with the stability of the imidazolyl anions; regioselective carbodesilylation in 2-, 5-, or 4-position of the twofold TMS-substituted imidazoles 3a and 9 therefore is possible, which allows the synthesis of a great variety of hydroxyalkyl-substituted imidazoles and of acylimidazoles.By using the dimethylsulfamoyl substituent as an N-protecting group, the N-unsubstituted 5-benzoylimidazole (26) as well as the comparable 5-benzoyl-pyrazole (30b) and 5-(hydroxyphenylmethyl)pyrazole (30a) are accessible. Key Words : Imidazoles, (trimethylsilyl)-, carbodesilylation of / Pyrazoles, (trimethylsilyl)-, carbodesilylation of / Carbodesilylation

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