59865-16-6 Usage
Description
30-ethyl-34-[(Z)-hex-4-en-2-yl]-4,7,10,12,15,19,25,28-octamethyl-33-methylamino-6,9,18,24-tetrakis(2-methylpropyl)-3,21-dipropan-2-yl-1-oxa-4,7,10,13,16,19,22,25,28,31-decazacyclotetratriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone is a complex organic compound with a long and intricate chemical structure. It is characterized by its multiple methyl, ethyl, and propyl groups, as well as its unique arrangement of carbon atoms and functional groups.
Uses
Used in Pharmaceutical Industry:
30-ethyl-34-[(Z)-hex-4-en-2-yl]-4,7,10,12,15,19,25,28-octamethyl-33-methylamino-6,9,18,24-tetrakis(2-methylpropyl)-3,21-dipropan-2-yl-1-oxa-4,7,10,13,16,19,22,25,28,31-decazacyclotetratriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone is used as an active pharmaceutical ingredient for the development of new drugs targeting various medical conditions. Its complex structure and unique functional groups make it a promising candidate for drug discovery and design.
Used in Chemical Research:
30-ethyl-34-[(Z)-hex-4-en-2-yl]-4,7,10,12,15,19,25,28-octamethyl-33-me thylamino-6,9,18,24-tetrakis(2-methylpropyl)-3,21-dipropan-2-yl-1-oxa4,7,10,13,16,19,22,25,28,31-decazacyclotetratriacontane-2,5,8,11,14,17 ,20,23,26,29,32-undecone is also used as a research tool in the field of organic chemistry, particularly for studying the synthesis, reactivity, and properties of complex organic molecules. Its unique structure and functional groups can provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Used in Material Science:
30-ethyl-34-[(Z)-hex-4-en-2-yl]-4,7,10,12,15,19,25,28-octamethyl-33-me thylamino-6,9,18,24-tetrakis(2-methylpropyl)-3,21-dipropan-2-yl-1-oxa4,7,10,13,16,19,22,25,28,31-decazacyclotetratriacontane-2,5,8,11,14,17 ,20,23,26,29,32-undecone's intricate structure and diverse functional groups make it a potential candidate for the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. It can be used in the design and synthesis of novel materials for various applications, including catalysis, sensors, and energy storage.
Used in Cyclosporin A Analysis:
As a rearranged degradation product of cyclosporin A, this compound can be used in the development of high-performance liquid chromatography (HPLC) fluorescence methods for quantifying cyclosporin A. This application can be particularly useful in the pharmaceutical industry for quality control and monitoring the stability of cyclosporin A in drug formulations.
Used in Cyclosporin A Impurity Analysis:
30-ethyl-34-[(Z)-hex-4-en-2-yl]-4,7,10,12,15,19,25,28-octamethyl-33-methylamino-6,9,18,24-tetrakis(2-methylpropyl)-3,21-dipropan-2-yl-1-oxa-4,7,10,13,16,19,22,25,28,31-decazacyclotetratriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone can be used as a reference compound for the identification and quantification of cyclosporin A impurities. This application is crucial for ensuring the purity and safety of cyclosporin A in pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 59865-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59865-16:
(7*5)+(6*9)+(5*8)+(4*6)+(3*5)+(2*1)+(1*6)=176
176 % 10 = 6
So 59865-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C62H111N11O12/c1-25-27-28-40(15)52-50(63-18)56(78)66-43(26-2)58(80)68(19)33-48(74)69(20)44(29-34(3)4)55(77)67-49(38(11)12)61(83)70(21)45(30-35(5)6)54(76)64-41(16)53(75)65-42(17)57(79)71(22)46(31-36(7)8)59(81)72(23)47(32-37(9)10)60(82)73(24)51(39(13)14)62(84)85-52/h25,27,34-47,49-52,63H,26,28-33H2,1-24H3,(H,64,76)(H,65,75)(H,66,78)(H,67,77)/b27-25-
59865-16-6Relevant articles and documents
1H NMR analysis of isocyclosporin A prepared in organic solvent and in aqueous solution
Arnoldi, Lolita,Manzocchi, Ada,Magni, Fulvio,Del Puppo, Marina,Galli Kienle, Marzia
, p. 110 - 116 (1997)
Isocyclosporins are isomers of cyclosporins deriving from an N,O-acyl transfer occurring under acidic conditions. For the identification by 1H NMR of isocyclosporins prepared in organic solvents the signal at 2.3 ppm assigned to three hydrogens of the NHCH3 group is considered. Results reported here show that the 1H NMR spectrum of isocyclosporin A prepared in aqueous acidic conditions lacks of the above signal and profoundly differs from that of isocyclosporin A prepared in organic solvents, despite the identity of the primary structures determined on the basis of mass spectrometric analysis.
Isolation and structure determination of the new cyclosporins E, F, G, H and I
Traber,Loosli,Hofmann,et al.
, p. 1655 - 1677 (1982)
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