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[17-(Diethoxy-phosphoryl)-2,16-dioxo-4,18-bis-((E)-styryl)-1,15-dioxa-cyclooctacos-3-yl]-phosphonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137151-53-2

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137151-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137151-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,1,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137151-53:
(8*1)+(7*3)+(6*7)+(5*1)+(4*5)+(3*1)+(2*5)+(1*3)=112
112 % 10 = 2
So 137151-53-2 is a valid CAS Registry Number.

137151-53-2Downstream Products

137151-53-2Relevant academic research and scientific papers

Synthesis of a novel type of chiral phosphinocarboxylic acids. The phosphine-palladium complexes catalyzed asymmetric allylic alkylation

Okada,Minami,Umezu,Nishikawa,Mori,Nakayama

, p. 667 - 682 (1991)

A novel type of chiral cycloalkylphosphines bearing the carboxy group at the β-position were developed, and used for palladium catalyzed asymmetric allylic alkylation of allylic substrates such as 2-cyclohexenylacetate and 1,3-disubstituted-propenyl acetates (R1CH=CHCH(OAc)R2:R1=R2=Ph; R1=Ph, R2=(CH2)4OAc; R1=Ph, R2=(CH2)6OAc; R1=Ph, R2=(CH2)10OAc). Reaction of the propenyl acetates with soft carbon nucleophiles such as triethyl sodiophosphonoacetate and sodiomalonic acid esters in the presence of a palladium catalyst prepared in situ from Pd(OAc)2 and chiral (2-diphenylphospino)cycloalkanecarboxylic acids (7a,b) gave high yields of alkylation products (PhCH=CHCH(X)Ph: > 77%ee for X=CH(CO2Et)P(O)(OEt)2 and >72 %ee for X=CH(CO2Me)2. The alkylation products 15 and 28a-c were converted into optically active α-methylene-γ-lactone and α-methylene macrolide derivatives. The high stereoselectivity demonstrated by the chiral phosphinocarboxylic acid-palladium catalyzed allylic alkylation suggested to be caused by an electronic repulsion between the carboxy group on the ligand and the incoming soft carbon nucleophile, which directs the nucleophilic attack on one of the π-allyl carbons.

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