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tert-butyl [(3R,4S)-3-[(2R)-2-hydroxy-4-methylpentanamido]-2,6-dimethylheptan-4-yl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1596798-34-3

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1596798-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1596798-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,6,7,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1596798-34:
(9*1)+(8*5)+(7*9)+(6*6)+(5*7)+(4*9)+(3*8)+(2*3)+(1*4)=253
253 % 10 = 3
So 1596798-34-3 is a valid CAS Registry Number.

1596798-34-3Downstream Products

1596798-34-3Relevant academic research and scientific papers

Synthesis and cytotoxicity of the proposed structure of piperazirum, its stereoisomers and analogues

Sudhakar, Gangarajula,Bayya, Shruthi,Reddy, Karla Janardhan,Sridhar, Balasubramanian,Sharma, Komal,Bathula, Surendar Reddy

, p. 1253 - 1265 (2014/03/21)

Piperazirum, a new biologically active alkaloid isolated from Arum palaestinum Bioss, is described, starting from commercially available α-amino acids. Two synthetic strategies were developed for the synthesis of the enantiomeric pair of compounds corresponding to the proposed structure of piperazirum. The first strategy was used in the synthesis of stereoisomers, and the second one was used in generating the analogues. The compounds synthesized were screened against different cell lines to evaluate their cytotoxicity profiles. Piperazirum, its stereoisomers, and its analogues were synthesized and tested for their antiproliferative activity. Copyright

Synthesis and Cytotoxicity of the Proposed Structure of Piperazirum, Its Stereoisomers and Analogues

Sudhakar, Gangarajula,Bayya, Shruthi,Reddy, Karla Janardhan,Sridhar, Balasubramanian,Sharma, Komal,Bathula, Surendar Reddy

, p. 1253 - 1265 (2015/10/05)

Piperazirum, a new biologically active alkaloid isolated from Arum palaestinum Bioss, is described, starting from commercially available α-amino acids. Two synthetic strategies were developed for the synthesis of the enantiomeric pair of compounds corresponding to the proposed structure of piperazirum. The first strategy was used in the synthesis of stereoisomers, and the second one was used in generating the analogues. The compounds synthesized were screened against different cell lines to evaluate their cytotoxicity profiles.

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