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N,N-diethyl-4-methylselenobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160594-72-9

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160594-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160594-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,9 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 160594-72:
(8*1)+(7*6)+(6*0)+(5*5)+(4*9)+(3*4)+(2*7)+(1*2)=139
139 % 10 = 9
So 160594-72-9 is a valid CAS Registry Number.

160594-72-9Downstream Products

160594-72-9Relevant academic research and scientific papers

Facile synthesis of N,N-dialkylselenoamides from amides

Koketsu, Mamoru,Okayama, Yoshihiro,Aoki, Hiroshi,Ishihara, Hideharu

, p. 195 - 198 (2002)

The synthesis of the N,N-dialkylselenoamides from amides was discussed. These selenoamides were chlorinated with oxalyl chloride and then they were allowed to react with LiAlHSeH to afford the corresponding N,N-dialkylamides in moderate to good yields. Af

Tertiary selenoamide compounds are useful superoxide radical scavengers in vitro

Takahashi, Hitoe,Nishina, Atsuyoshi,Kimura, Hirokazu,Motoki, Kenji,Koketsu, Mamoru,Ishihara, Hideharu

, p. 207 - 211 (2007/10/03)

We investigated the scavenging effects of tertiary selenoamide compounds for super oxide radicals using a highly sensitive and quantitative chemiluminescence method. At 333 nM, tertiary selenoamide compounds scavenged 25.8-81.6% of O2-/su

A Willgerodt-Kindler Type Selenation of Dihalomethane Derivatives, Chloroform, and Sodium Trichloroacetate by Treating with a Base, Elemental Selenium, and an Amine

Shimada, Kazuaki,Yamaguchi, Minoru,Sasaki, Tohru,Ohnishi, Kenji,Takikawa, Yuji

, p. 2235 - 2242 (2007/10/03)

Treatment of dihalomethane derivatives, chloroform, or sodium trichloroacetate with elemental selenium in the presence of NaH and an excess amount of an amine gave the corresponding selenoamides, selenoureas, and bis(selenocarbamoyl) triselenides in modest yields. These products were afforded from reactive intermediates related to "selenocarbonyl halides" and "selenophosgenoids" generated by the reaction of dichloromethanide ions and trichloromethanide ion with N-alkylated aminopolyselenide species (R2N-(Se)n-).

Convenient Syntheses of N,N-Dialkylselenoamides and N,N,N',N'-Tetraalkylselenoureas by Treating Terminal gem-Dihaloalkanes, Chloroform , or Sodium Trichloroacetate with a Base, Elemental Selenium, and Amines

Takikawa, Yuji,Yamaguchi, Minoru,Sasaki, Tohru,Ohnishi, Kenji,Shimada, Kazuaki

, p. 2105 - 2108 (2007/10/02)

Treatment of terminal gem-dihaloalkanes, chloroform or sodium trichloroacetate with elemental selenium in the presence of NaH and an excess amount of primary or secondary amines gave selenoamides and selenoureas in modest yields.

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