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The chemical compound "(5S,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28E,30E,32S)-5,32-bis(1-hydroxy-1-methylethyl)-2,8,12,16,21,25,29,35-octamethylhexatriaconta-6,8,10,12,14,16,18,20,22,24,26,28,30-tridecaene-2,35-diol" is a complex, long-chain polyene alcohol with a unique structure. It features a hexatriaconta-tridecaene backbone, which is a 36-carbon chain with 13 double bonds, arranged in a specific pattern to ensure the correct geometry and stereochemistry. The compound also includes two hydroxyl groups at the 2nd and 35th carbon positions and eight methyl groups attached to the 2nd, 8th, 12th, 16th, 21st, 25th, 29th, and 35th carbons, contributing to its octamethyl characteristic. This specific arrangement of functional groups and carbon chain length gives the compound its unique properties and potential applications in various fields, such as pharmaceuticals or materials science.

556-80-9

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556-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556-80-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 556-80:
(5*5)+(4*5)+(3*6)+(2*8)+(1*0)=79
79 % 10 = 9
So 556-80-9 is a valid CAS Registry Number.

556-80-9Downstream Products

556-80-9Relevant academic research and scientific papers

36. C45- and C50-Carotenoids Part 81)Synthesis of (all-E,25,2′S)-Bacterioruberin, (all-E,2S,2′S)-Monoanhydrobacterioruberin, (all-E,2S,2′S)Bisanhydrobacterioruberin, (all-E,2R,2′R)-3,-Tetrahydrobisanhydro- bacterioruberin, and (all-E,S)-2-Isopentenyl-3,4-dehydrorhodopin

Lakomy, Ivo,Sarbach, Daniel,Traber, Bruno,Arm, Christoph,Zuber, Daniel,Pfaender, Hanspeter,Noack, Klaus

, p. 472 - 486 (2007/10/03)

Starting from (R)-3-hydroxybutyric acid ((R)-10) the C45- and C50-carotenoids (all-E,25,2′S)-bacterioruberin (1), (all-E,2S,2′S)-monoanhydrobacterioruberin (2), (all-E,2S,2′S)-bisanhydrobacterioruberin (3), (all-E,2R,2′R)-3,4,3′,4′-tetrahydrobisanhydrobacterioruberin (5), and (all-E,S)-2-isopentenyl-3-4-dehydrorhodopin (6) were synthesized. By comparison of the chiroptical data of the natural and the synthetic compounds, the (2S)- and (2'S)-configuration of the natural products 1-3 and 6 was established.

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