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ETHYL 5-OXO-5-(2-PYRIDYL)VALERATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898776-54-0

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898776-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898776-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,7 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 898776-54:
(8*8)+(7*9)+(6*8)+(5*7)+(4*7)+(3*6)+(2*5)+(1*4)=270
270 % 10 = 0
So 898776-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-2-16-12(15)8-5-7-11(14)10-6-3-4-9-13-10/h3-4,6,9H,2,5,7-8H2,1H3

898776-54-0Downstream Products

898776-54-0Relevant academic research and scientific papers

Inorganic alkali catalytic 1, 5 - ketonic ester apperception compound synthesis method

-

Paragraph 0051-0053, (2017/10/11)

The invention discloses a synthesis method for a 1,5-ketonic ester compound under catalyzing of inorganic base. The synthesis method comprises the following steps: taking a compound of the general formula I as a raw material, taking inorganic base as a ca

Sequential Michael addition/retro-Claisen condensation of aromatic β-diketones with α,β-unsaturated esters: An approach to obtain 1,5-ketoesters

Cai, Gui-Xin,Wen, Jing,Lai, Ting-Ting,Xie, Dan,Zhou, Cheng-He

supporting information, p. 2390 - 2394 (2016/03/01)

A K2CO3-catalyzed one-pot protocol involving sequential C-C bond formation and cleavage of aromatic β-diketones with α,β-unsaturated esters is developed to obtain 1,5-ketoesters. The sequential reaction via Michael addition and retro-Claisen condensation proceeds smoothly under mild conditions in up to 98% isolated yield. The mechanism study disclosed that the cascade process involved C-C bond cleavage of aromatic β-diketone as a phenacyl donor under alcoholic alkalescent conditions.

Catalytic asymmetric hydrogenation of δ-ketoesters: Highly efficient approach to chiral 1,5-diols

Yang, Xiao-Hui,Xie, Jian-Hua,Liu, Wei-Peng,Zhou, Qi-Lin

, p. 7833 - 7836 (2013/08/23)

High turnover: An highly efficient catalytic asymmetric hydrogenation of δ-aryl-δ-ketoesters has been realized by using the chiral spiroiridium catalyst (R)-1. Chiral 1,5-diol products are obtained with excellent enantioselectivity and turnover numbers (TONs) as high as 100 000. TOF=turnover frequency. Copyright

A series of thiazole derivatives bearing thiazolidin-4-one as non-competitive ADAMTS-5 (aggrecanase-2) inhibitors

Atobe, Masakazu,Maekawara, Naomi,Ishiguro, Noriko,Sogame, Shinya,Suenaga, Yoshihito,Kawanishi, Masashi,Suzuki, Hiroko,Jinno, Norimasa,Tanaka, Eiichi,Miyoshi, Shiro

, p. 2106 - 2110 (2013/04/24)

A series of thiazole bearing thiazolidin-4-one was discovered via high-throughput screening as non-competitive inhibitors of ADAMTS-5. Compound 31 appeared to give the best ADAMTS-5 inhibition and good selectivity over other metalloproteases.

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