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65928-85-0

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65928-85-0 Usage

Description

(3beta)-cholest-5-en-3-yl carbonofluoridate, also known as cholesteryl fluorocarbonate, is a cholesterol-derived chemical compound formed by the reaction of cholesterol with carbonofluoridic acid. It features a carbonofluoride group attached to the 3rd carbon of the cholesteryl side chain, making it a unique derivative with potential applications in various fields.

Uses

Used in Drug Delivery Systems:
(3beta)-cholest-5-en-3-yl carbonofluoridate is used as a component in the synthesis of novel lipids for drug delivery systems. Its unique structure allows for the development of lipid-based carriers that can enhance the delivery and bioavailability of therapeutic agents.
Used in Lipid Organization Studies:
In the field of membrane biology, (3beta)-cholest-5-en-3-yl carbonofluoridate serves as a probe for studying lipid organization in model and biological membranes. This helps researchers understand the behavior and interactions of lipids within cellular environments.
Used in Lipid Metabolism Research:
(3beta)-cholest-5-en-3-yl carbonofluoridate is utilized in the study of lipid metabolism, providing insights into the processes and pathways involved in lipid synthesis, transport, and breakdown.
Used in Pharmaceutical Development:
With its potential applications in the development of new pharmaceuticals, (3beta)-cholest-5-en-3-yl carbonofluoridate contributes to the discovery and design of innovative drugs that can address various health conditions.
Used in Biomedical Materials:
(3beta)-cholest-5-en-3-yl carbonofluoridate may also find use in the development of biomedical materials, where its unique properties can be harnessed to create advanced materials for medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65928-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,2 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65928-85:
(7*6)+(6*5)+(5*9)+(4*2)+(3*8)+(2*8)+(1*5)=170
170 % 10 = 0
So 65928-85-0 is a valid CAS Registry Number.

65928-85-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Cholest-5-en-3-ol (3b)-, carbonofluoridate (9CI)

1.2 Other means of identification

Product number -
Other names cholesterol n-dodecanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65928-85-0 SDS

65928-85-0Upstream product

65928-85-0Downstream Products

65928-85-0Relevant articles and documents

Process for the preparation of fluoroformates

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, (2008/06/13)

A process for the preparation of fluoroformates of formula: STR1 in which R1 is a substituted or unsubstituted, saturated or unsaturated aliphatic, cycloaliphatic or polycyclic radical, or substituted or unsubstituted araliphatic radical or an aromatic radical, which consists of reacting a carbonate of formula: STR2 in which R1 has the same meaning as hereinabove and R2 is hydrogen, alkyl of 1-12 carbon atoms, cycloalkyl of 5-12 carbon atoms, saturated or unsaturated, unsubstituted or substituted by one or more halogen atoms or R2 is aryl, unsubstituted or substituted by one or more halogen atoms, with an alkali or alkaline earth fluoride, ammonium fluoride or a quaternary ammonium fluoride, of formula FNR3 R4 R5 R6, wherein R3, R4, R5, R6 are the same or different and are hydrogen, alkyl or aralkyl of 1-12 carbon atoms or a fluoride which is KHF2, NH4 HF2 or KSO2 F. The fluoride is activated by a complexing agent for the cation which is a cryptate, a cyclic or linear polyether or by means of a polar aprotic compound. The carbonate is split to give a reaction mixture containing an aldehyde and the fluoroformate which is removed from the reaction mixture.

Preparation of steroid haloformate esters

Nakanishi,Jensen

, p. 3398 - 3400 (2007/10/17)

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