Interesting facts
Interesting Facts About (3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
This complex organic compound is structurally rich and falls under the category of steroids, which are known for their significant roles in biology and chemistry. Below are some compelling aspects of this compound:
- Steroidal Framework: The intricate arrangement of its rings is reflective of steroidal compounds, which makes this compound possibly influential in hormone-related studies.
- Chirality: Notably, this molecule contains multiple chiral centers, as indicated by its elaborate stereochemistry (3S, 8S, 9S, etc.). This presents a fascinating opportunity for examining stereoisomerism and the effects of different spatial arrangements on biological activity.
- Biological Relevance: Compounds of this nature can have profound implications in pharmacology, particularly in the development of therapeutics addressing various health conditions, including hormonal imbalances.
- Natural Inspiration: The structure hints at a potential natural source or inspiration, possibly derived from plant steroids or as a synthetic analog with larger biological implications.
- Research Opportunities: Researchers can explore this compound’s properties as it may serve as a starting point for the synthesis of derivatives with enhanced or modified properties.
As a student or scientist, delving into the properties and applications of such intricate compounds offers not just knowledge but also the potential for discovery. As Albert Einstein famously said, "The important thing is not to stop questioning." Keeping this in mind, the synthesis and function of compounds like this can open myriad paths for inquiry and innovation in organic and medicinal chemistry.
Synonyms
cholesterol
57-88-5
Cholesterin
Cholest-5-en-3beta-ol
Cholesteryl alcohol
Dythol
Cholestrin
Cordulan
Dusoline
Dusoran
Cholesterine
Cholestrol
Hydrocerin
Lidinite
Kathro
Lanol
Super hartolan
Lidinit
Cholesterol base H
Provitamin D
Nimco cholesterol base H
(-)-Cholesterol
Cholesterinum
Tegolan
5:6-Cholesten-3beta-ol
3beta-Hydroxycholest-5-ene
Tegolan (VAN)
Cholest-5-en-3-beta-ol
5-Cholesten-3beta-ol
(3beta)-cholest-5-en-3-ol
CCRIS 2834
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Cholest-5-en-3-ol (3beta)-
HSDB 7106
Cholest-5-en-3-ol
3beta-Hydroxy-5-cholestene
NSC 8798
3-beta-Hydroxycholest-5-ene
5-Cholesten-3B-ol
Cholest-5-en-3-ol (3.beta.)-
Dastar
CHEBI:16113
Provitamin-d
Cholest-5-en-3-ol, (3beta)-
AI3-03112
delta(sup 5)-Cholesten-3-beta-ol
Fancol CH
NSC-8798
3h-cholesterol
EINECS 200-353-2
UNII-97C5T2UQ7J
97C5T2UQ7J
DTXSID3022401
Nimco cholesterol base No. 712
NSC8798
5-cholestene-3beta-ol
Cholesterol (Excipient)
5:6-Cholesten-3-ol
(3beta,14beta,17alpha)-cholest-5-en-3-ol
MFCD00003646
5-Cholesten-3.beta.-ol
Cholest-5-en-3.beta.-ol
5,6-Cholesten-3.beta.-ol
3.beta.-Hydroxycholest-5-ene
DTXCID402401
EC 200-353-2
129111-15-5
NCGC00159351-02
CHOLESTEROL (II)
CHOLESTEROL [II]
CHOLESTEROL (IARC)
CHOLESTEROL [IARC]
CHOLESTEROL (MART.)
CHOLESTEROL [MART.]
CHOLESTEROL (USP-RS)
CHOLESTEROL [USP-RS]
CHOLESTEROL (EP MONOGRAPH)
CHOLESTEROL [EP MONOGRAPH]
Cholesterol-t
(3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
(3H)-Cholesterol
epicholesterin
Cholesterol [BAN:JAN:NF]
Cholesterol?
.DELTA.5-Cholesten-3-.beta.-ol
80356-14-5
1zhy
Cholesterol,(S)
Cholest-5-en-3-ol, (3.beta.)- #
Cholesterol1551
Cholesterol (TN)
20-epi-cholesterol
20-iso-cholesterol
Cholesterol, 94%
Liquid crystal CN/9
(+)-ent-Cholesterol
cholest-5-en-3b-ol
5-Cholesten-3ss--ol
Cholesterol (Standard)
Cholesterol (>99%)
Cholesterol, 99.0%
CHOLESTEROL [MI]
ALF component cholesterol
CHOLESTEROL [JAN]
ALFQ component cholesterol
Cholesterol (JP18/NF)
CHOLESTEROL [HSDB]
Phospholipon & Cholesterol
Delta5-Cholesten-3beta-ol
Epitope ID:150761
CHOLESTEROL [VANDF]
3beta-cholest-5-en-3-ol
3ss--Hydroxy-5-cholestene
ALF43 component cholesterol
CHOLESTERINUM [HPUS]
BIDD:PXR0095
(3b)-cholest-5-en-3-ol
CHOLESTEROL [WHO-DD]
5:6-Cholesten-3.beta.-ol
20bFH-cholest-5-en-3b-ol
BIDD:ER0548
Cholest-5-en-3-ol (3beta)-, labeled with tritium
CHEMBL112570
Cholest-5-en-3-ol (3beta)
GTPL2718
BDBM20192
HY-N0322B
HY-N0322R
(20bFH)-cholest-5-en-3b-ol
CHEBI:140435
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
Cholesterol, Sigma Grade, >=99%
HY-N0322
Tox21_111595
CMC_13392
LMST01010001
s4154
AKOS005267135
Cholest-5-en-3-ol, (3-.beta.)-
CS-5106
DB04540
FC28806
GS-6857
CAS-57-88-5
Cholesterol, NIST(R) SRM(R) 911c
SMP1_000069
NCGC00159351-03
22243-67-0
BP-26125
Cholesterol 10 microg/mL in Acetonitrile
Cholesterol, tested according to Ph.Eur.
C3624
Cholesterol, from lanolin, >=95.0% (GC)
Cholesterol, from lanolin, >=99.0% (GC)
CS-1096707
NS00005787
Army Liposome Formulation component cholesterol
C00187
D00040
EN300-323186
F70214
Q43656
AB00443913_03
Cholesterol, >=95% (GC), powder, Ash, free
Cholesterol, Vetec(TM) reagent grade, >=92.5%
Soya phospholipon & Cholesterol (2:1 molar ratio)
5BBA213B-ECF4-44AF-8AAF-8A0120F2F886
WLN: L E5 B666 LUTJ A1 E1 FY1&3Y1&1 OQ
Z2033589790
Cholesterol, powder, BioReagent, suitable for cell culture, >=99%
Cholesterol, United States Pharmacopeia (USP) Reference Standard
Cholesterol, Pharmaceutical Secondary Standard; Certified Reference Material
(1R,3aS,3bS,7S,9aR,9bS,11aR)-9a,11a-dimethyl-1-[(2R)-6-methylheptan-2-yl]-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ol
200-353-2
Solubility of (3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Understanding the solubility of complex organic molecules like C27H44O can be quite intriguing. This compound, being a member of the steroid family, tends to exhibit unique solubility characteristics. Here are some key points to consider:
In essence, while solubility is influenced by molecular structure and interactions with solvents, the characteristics of C27H44O suggest it is best practiced in non-polar solvents rather than polar ones. Understanding these relationships not only aids in practical applications but also enhances our overall comprehension of chemical behavior.