3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene is a steroid compound belonging to the cholest-5-ene derivatives class. It features a cholest-5-ene core structure with an attached iodohexyl group, which may contribute to its unique properties and potential applications in various chemical and biological studies.
68354-86-9
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Basic information
- Product Name: 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene
- Synonyms: 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene
- CAS NO:68354-86-9
- Molecular Formula: C33H57IO
- Molecular Weight: 596.719
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene(CAS DataBase Reference)
- NIST Chemistry Reference: 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene(68354-86-9)
- EPA Substance Registry System: 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene(68354-86-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 68354-86-9(Hazardous Substances Data)
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68354-86-9 Usage
Uses
Used in Pharmaceutical Development:3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene is used as a research tool for studying the effects and interactions of steroid compounds in biological systems. Its unique structure and properties make it valuable in the development of pharmaceuticals targeting steroid signaling pathways.
Used in Disease Mechanism Research:
In the field of medical research, 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene is used as a research compound to understand the mechanisms of diseases or conditions that involve steroid signaling pathways. Its presence in biological systems can provide insights into the role of steroid compounds in these conditions.
Used in Chemical Studies:
3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene is also used in chemical studies to explore its properties and potential applications. The iodine atom in the molecule may offer unique chemical reactivity or interactions with other molecules, making it a valuable subject for further investigation in the chemical sciences.
Used in Drug Delivery Systems:
Although not explicitly mentioned in the provided materials, the potential use of 3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene in drug delivery systems can be inferred. Its unique structure and properties may allow for the development of novel drug delivery systems, enhancing the delivery, bioavailability, and therapeutic outcomes of pharmaceuticals targeting steroid signaling pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 68354-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.Calculate Digit Verification of CAS Registry Number 68354-86:
(7*6)+(6*8)+(5*3)+(4*5)+(3*4)+(2*8)+(1*6)=159
159 % 10 = 9
So 68354-86-9 is a valid CAS Registry Number.
68354-86-9Upstream product
68354-86-9Downstream Products
- 68354-92-7 6-(5-cholesten-3β-yloxy)hexyl 1-thio-β-D-mannopyranoside
- 87171-81-1 6-(5-cholesten-3β-yloxy)hexyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl--4-O-benzoyl-6-deoxy-β-D-galactopyranosyl)-1-thio-β-D-glucopyranoside
- 87171-74-2 6-(5-cholesten-3β-yloxy)hexyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-β-D-galactopyranosyl)-1-thio-β-D-glucopyranoside
- 68354-92-7 6-(5-cholesten-3β-yloxy)hexyl 1-thio-β-D-glucopyranoside
- 103003-27-6 cholest-5-en-3β-yl 6-<(p-carboxybenzyl)thio>hexyl ether succinimido ester
- 103003-26-5 cholest-5-en-3β-yl 6-<(p-carboxybenzyl)thio>hexyl ether
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3-[(6-Iodohexyl)oxy]-(3b)-cholest-5-ene
