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(1R)-1,2,3,4,4a,9,10,10aα-Octahydro-4α-hydroxy-1,4aβ-dimethyl-7-isopropyl-1-phenanthrenemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24338-63-4

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24338-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24338-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24338-63:
(7*2)+(6*4)+(5*3)+(4*3)+(3*8)+(2*6)+(1*3)=104
104 % 10 = 4
So 24338-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O2/c1-13(2)14-5-7-16-15(11-14)6-8-17-19(3,12-21)10-9-18(22)20(16,17)4/h5,7,11,13,17-18,21-22H,6,8-10,12H2,1-4H3/t17?,18-,19-,20+/m0/s1

24338-63-4Upstream product

24338-63-4Downstream Products

24338-63-4Relevant academic research and scientific papers

Lophachinins A–E, abietane diterpenes from a Mongolian traditional herbal medicine Lophanthus chinensis

Damdinjav, Davaadagva,Dorjval, Enkhjargal,Itoh, Kohji,Kashiwada, Yoshiki,Kawazoe, Kazuyoshi,Shimomoto, Yusei,Tanaka, Naonobu,Tsuji, Daisuke,Yamada, Kenta

, (2020)

Five new abietane diterpenes, lophachinins A–E (1–5), and eleven known related diterpenes were isolated from a Mongolian traditional herbal medicine, the aerial parts of Lophanthus chinensis (Lamiaceae). The structures of new diterpenes were assigned by spectroscopic analyses. Lophachinins A (1) and B (2) were abietane diterpene possessing an endoperoxy bridge at C-ring. In contrast, lophachinins C–E (3–5) had an abietane skeleton with an aromatized C-ring. The absolute configuration of 1 was elucidated by application of the modified Mosher's method, while those of 2, 3, and 5 were assigned by chemical conversions. The absolute configuration of lophachinin D (4) was deduced by ECD calculation. Anti-inflammatory activity of isolated diterpenes on microglial cells were evaluated.

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