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1,2-(4H)-pyridinedicarboxylic acid 5, 6-dihydro-2-methyl-1-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1359711-06-0

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1359711-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1359711-06-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,7,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1359711-06:
(9*1)+(8*3)+(7*5)+(6*9)+(5*7)+(4*1)+(3*1)+(2*0)+(1*6)=170
170 % 10 = 0
So 1359711-06-0 is a valid CAS Registry Number.

1359711-06-0Relevant articles and documents

Synthesis of cis- and trans-(±)-3-mercaptoproline and pipecolic acid derivatives via thio-Michael addition

Gutiérrez, Alejandro,Osante, I?aki,Cativiela, Carlos

, p. 1661 - 1665 (2018)

The reactivity of 2,3-dehydroproline and 2,3-dehydropipecolic acid methyl ester derivatives with S-nucleophiles in the thio-Michael addition reaction has been explored. The addition of triphenylmethanethiol and subsequent trityl cleavage led to the corres

A novel method for the synthesis of 3,4-disubstitutedpyrrole-2,5- dicarboxylates from hydrazones derived from α-diazo esters

Yasui, Eiko,Wada, Masao,Nagumo, Shinji,Takamura, Norio

, p. 4325 - 4330 (2013/06/27)

Hydrazones obtained from α-diazo esters were converted to pyrroles when heated with thionyl chloride in alcohol. Among hydrazones, those substituted with a benzene ring on the β-carbon to the ester are likely to give pyrroles in good yields.

Diastereodivergent synthesis of 4-hydroxy-2,3-methanopipecolic acid derivatives as conformationally constrained homoserine analogues

Occhiato, Ernesto G.,Casini, Andrea,Guarna, Antonio,Scarpi, Dina

experimental part, p. 6544 - 6552 (2012/01/06)

A short, practical procedure for the diastereodivergent synthesis of cyclopropanated 4-hydroxypipecolic acid derivatives with high optical purity is reported. Key steps are the highly enantioselective lipase-catalyzed kinetic resolution and the stereosele

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