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Benzoic acid, 3-formyl-2-pentyl-4,6-bis(phenylmethoxy)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64750-24-9

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64750-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64750-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64750-24:
(7*6)+(6*4)+(5*7)+(4*5)+(3*0)+(2*2)+(1*4)=129
129 % 10 = 9
So 64750-24-9 is a valid CAS Registry Number.

64750-24-9Relevant academic research and scientific papers

METHOD FOR SYNTHESIS OF LOBARIC ACID AND ANALOG THEREOF

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, (2021/08/13)

The present invention can synthesize lobaric acid and four analogues thereof, which are five phenolic lichen metabolites isolated from an extract of the Antarctic lichen Stereocaulon alpinum and selectively inhibit PTP1B, by a simple, economic and efficient chemical synthesis method.

Total Syntheses of Lobaric Acid and Its Derivatives from the Antarctic Lichen Stereocaulon alpinum

Kim, Tai Kyoung,Kim, Joung Eun,Youn, Ui Joung,Han, Se Jong,Kim, Il-Chan,Cho, Cheon-Gyu,Yim, Joung Han

, p. 1460 - 1467 (2018/06/29)

The first total syntheses of the natural products lobaric acid (1) and its derivatives isolated from the Antarctic lichen Stereocaulon alpinum are reported in this study. Lobarin (3), with a pseudodepsidone structure, was synthesized first in 11 steps by utilizing an Ullmann aryl ether coupling reaction, and lobaric acid was synthesized in an additional three steps by a seven-membered lactonization reaction. Various derivatives were also obtained from the prepared lobaric acid, and the synthetic compounds exhibited significant PTP1B inhibitory activities.

Synthesis of Further Lichen Depsides

Elix, John A.,Barclay, Caroline E.,David, Feeya,Griffin, Frank K.,Hill, Alison M.,et al.

, p. 301 - 313 (2007/10/02)

The unambiguous total synthesis of 18 lichen depsides has been achieved by the condensation of an appropriately substituted orsellinic acid and protected phenol in the key step, followed by subsequent deprotection and/or secondary reduction.The natural oc

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