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3-methyl-4-(phenylthiol)-1-butyn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150587-32-9

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150587-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150587-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,5,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150587-32:
(8*1)+(7*5)+(6*0)+(5*5)+(4*8)+(3*7)+(2*3)+(1*2)=129
129 % 10 = 9
So 150587-32-9 is a valid CAS Registry Number.

150587-32-9Downstream Products

150587-32-9Relevant academic research and scientific papers

Ruthenium-catalyzed oxidative transformations of terminal alkynes to ketenes by using tethered sulfoxides: Access to β-lactams and cyclobutanones

Wang, Youliang,Zheng, Zhitong,Zhang, Liming

supporting information, p. 9572 - 9576 (2014/10/15)

The oxidation of in situ generated Ru vinylidenes to ketenes is realized with tethered sulfoxides. The result is a Ru-catalyzed oxidative transformation of terminal alkynes to highly valuable ketenes. Moreover, the ketenes generated here were shown to und

-Sigmatropic Rearrangement of β-Phenylsulfonyl Propargylic Sulfenates as a Method for Preparing 1,4-Bis(phenylsulfonyl)-1,3-butadienes

Wang, Xiaoheng,Ni, Zhijie,Lu, Xiujing,Hollis, Andrea,Banks, Harold,et al.

, p. 5377 - 5385 (2007/10/02)

Several β-sulfoxy-substituted acetylenic carbinols were prepared by the addition of thiyl radicals and oxygen to conjugated enynes.The products obtained are derived from thiyl radical attack at the olefinic bond to generate a propargylic radical.Capture o

The co-oxidation of conjugated enynes. A convenient synthesis of β-sulfoxy acetylenic carbinols

Wang, Xiaoheng,Ni, Zhijie,Lu, Xiujing,Smith, Temeika Y.,Rodriguez, Augusto,Padwa, Albert

, p. 5917 - 5920 (2007/10/02)

Several β-sulfoxy substituted acetylenic carbinols were prepared by the addition of thiyl radicals and oxygen to conjugated enynes.

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