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Spiro[1,3-dioxolane-2,3'-[5α]cholestane] is a complex organic compound characterized by a unique spiro structure, which consists of two rings sharing a common atom. The compound features a 1,3-dioxolane ring fused to a cholestane backbone, with the cholestane being a steroidal structure. The 5α-cholestane indicates that the hydroxyl group is positioned at the 5th carbon in an alpha configuration. Spiro[1,3-dioxolane-2,3'-[5α]cholestane] is of interest in the field of organic chemistry, particularly in the synthesis of complex steroidal molecules and may have potential applications in pharmaceuticals or other industries where such structures are relevant. The specific properties and reactivity of Spiro[1,3-dioxolane-2,3'-[5α]cholestane] would depend on its molecular structure and the functional groups present, which can influence its behavior in chemical reactions and its potential uses.

1858-14-6

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1858-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1858-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1858-14:
(6*1)+(5*8)+(4*5)+(3*8)+(2*1)+(1*4)=96
96 % 10 = 6
So 1858-14-6 is a valid CAS Registry Number.

1858-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5α-cholestan-3-one ethylene ketal

1.2 Other means of identification

Product number -
Other names 3,3-ethanediyldioxy-5α-cholestane

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:1858-14-6 SDS

1858-14-6Downstream Products

1858-14-6Relevant academic research and scientific papers

Highly efficient heterogeneous acetalization of carbonyl compounds catalyzed by a titanium cation-exchanged montmorillonite

Kawabata, Tomonori,Mizugaki, Tomoo,Ebitani, Kohki,Kaneda, Kiyotomi

, p. 8329 - 8332 (2007/10/03)

The titanium cation-exchanged montmorillonite efficiently catalyzed the selective acetalization of various carbonyl compounds as a recyclable solid acid. This heterogeneous catalyst has an advantage of a strikingly simple workup procedure over conventional homogeneous acids.

Selective rhenium-catalyzed oxidation of secondary alcohols with methyl sulfoxide in the presence of ethylene glycol, a convenient one-pot synthesis of ketals

Arterburn, Jeffrey B.,Perry, Marc C.

, p. 769 - 771 (2008/02/12)

Formula presented Secondary alcohols are oxidized preferentially by DMSO and the catalyst ReOCl3(PPh3)2 in the presence of ethylene glycol and refluxing toluene, producing the corresponding ketals. The reactions are rapid, and proceed in very good to excellent yields. The byproducts of the reaction, methyl sulfide and water, are easily removed. No epoxidation or other common side reactions were observed. This direct oxidative transformation of alcohols to the protected ketal derivatives should have broad synthetic applicability.

A new selective catalytic acetalization method promoted by microwave irradiation

Kalita, Dipok J.,Borah, Ruli,Sarma, Jadab C.

, p. 4573 - 4574 (2007/10/03)

A new selective method of acetalization of aldehydes and cyclic ketones with 1,2-diols or alcohols catalyzed by iodine under microwave irradiation is reported.

Montmorillonite Clay Catalysis. Part 2. 1 An Efficient and Convenient Procedure for the Preparation of Acetals catalysed by Montmorillonite K-10

Li, Tong-Shuang,Li, Sheng-Hui,Li, Ji-Tai,Li, Hui-Zhang

, p. 26 - 27 (2007/10/03)

Acetalization of aldehydes and ketones is catalysed by montmorillonite K-10 in refluxing benzene or toluene in excellent yields.

Synthetic models for transmembrane channels: Structural variations that alter cation flux

Murillo, Oscar,Watanabe, Shigeru,Nakano, Akio,Gokel, George W.

, p. 7665 - 7679 (2007/10/03)

Twelve novel bis- or tris(macrocyclic) compounds have been designed as models for cation-conducting channels that function in phospholipid bilayer vesicle membranes. In general, the channel model systems have the structure "sidearm-crown-spacer-crown-spac

A New Ready, High-Yielding, General Procedure for Acetalization of Carbonyl Compounds

Caputo, Romualdo,Ferreri, Carla,Palumbo, Giovanni

, p. 386 - 389 (2007/10/02)

Carbonyl compounds are smoothly and rapidly acetalized by treatment with alcohols, in anhydrous acetonitrile, in the presence of polystyryl diphenyl phosphine - iodine complex as catalyst.Open and cyclic acetals, including 1,3-dioxolanes, 1,3-oxathiolanes, and 1,3-dithiolanes, of miscellaneous aldehydes and ketones have been successfully prepared in this way.The isolation of the product is very easily performed, by simple filtration of the polymer-linked phosphine oxide which is formed in the reaction.

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