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Silane, trimethyl[4-(4-methylphenyl)-3-furanyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148367-36-6

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148367-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148367-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,6 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148367-36:
(8*1)+(7*4)+(6*8)+(5*3)+(4*6)+(3*7)+(2*3)+(1*6)=156
156 % 10 = 6
So 148367-36-6 is a valid CAS Registry Number.

148367-36-6Relevant academic research and scientific papers

Regiospecific Displacement of the C-B Bond of Trisboroxines with C-Sn Bond and C-O Bond: Syntheses of 3,4-Disubstituted Furans and 4-Substituted-3(2H)-furanones

Song, Zhi Zhong,Wong, Henry N. C.

, p. 673 - 680 (2007/10/03)

Trisboroxines 2, prepared from the corresponding 4-(substituted)-3-(trimethylsilyl)furan 1, were converted successfully to 4-(substituted)-3-(tributylstannyl)furans 3 through palladium-catalyzed cross-coupling reactions with tri

3,4-Disubstituted Furans, 5. Regiospecific Mono-ipso-Iodination of 3,4-Bis(trimethylsilyl)furan and Regiospecific ipso-Iodination of Trisboroxines to 4-Substituted 3-(Trimethylsilyl)furans and Unsymmetrical 3,4-Disubstituted

Song, Zhi Zhong,Wong, Henry N. C.

, p. 29 - 34 (2007/10/02)

4-Iodo-3-trimethylsilylfuran (2), obtained through the regiospecific iodination of 3,4-bis(trimethylsilyl)furan (1), underwent either palladium- or nickel-catalyzed cross-coupling reactions with terminal alkenes, terminal alkynes, areneboronic acids, bis(

Synthesis and Reactions of 3,4-Bis(trimethylsilyl)furan: Diels-Alder Cycloaddition, Friedel-Crafts Acylation, and Regiospecific Conversion to 3,4-Disubstituted Furans

Song, Zhi Zhong,Ho, Mei Sing,Wong, Henry N. C.

, p. 3917 - 3926 (2007/10/02)

As a versatile building block, 3,4-bis(trimethylsilyl)furan (1), conveniently obtained through a Diels-Alder reaction between 4-phenyloxazole and bis(trimethylsilyl)acetylene, was able to undergo Diels-Alder cycloadditions with dienophiles.In two separate

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