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3,3-Ethylenedioxycholest-5-ene is a steroidal compound characterized by the presence of a cholestane core, which is a type of steroid nucleus. This molecule features a 5-ene double bond, indicating an unsaturated carbon-carbon bond at the 5th position. The ethylenedioxy group (-CH2OCH2-) is attached to the 3,3 positions, which are carbon atoms on the steroid ring structure. This specific arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's structure and properties make it a subject of interest for scientists studying steroidal compounds and their derivatives.

3496-88-6

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3496-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3496-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3496-88:
(6*3)+(5*4)+(4*9)+(3*6)+(2*8)+(1*8)=116
116 % 10 = 6
So 3496-88-6 is a valid CAS Registry Number.

3496-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]spiro[1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,2'-1,3-dioxolane]

1.2 Other means of identification

Product number -
Other names 3,3-Ethylenedioxycholest-5-ene

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:3496-88-6 SDS

3496-88-6Relevant academic research and scientific papers

Synthesis of 6-azacholesten-3-ones: Potent inhibitors of 5α-reductase

Haffner, Curt

, p. 4039 - 4042 (1995)

4-Cholesten-3-one was converted into 6-azacholesten-3-ones (7, 14 and 15). These compounds proved to be potent inhibitors of both type 1 and 2 human 5α-reductase.

Synthesis of deuterium and tritium labelled 7-hydroxy- and 7-oxosterols

Schabdach,Schroeder,Seifert

, p. 329 - 336 (1998)

Deuterium and tritium 3,7-bis-labelled 7-hydroxysterols 3 - 5 were prepared by reduction of the 3,7-dioxosterols 1, 2 with NaB2H4 and NaB3H4. Regioselective oxidation of the deuterium 3,7-bislabelled 7- hydroxysterols 3, 4 with CrO3/DMP led to the 3-labelled 7-oxosterols 6, 7. The 3,7-dioxosterols 1, 2 were synthesized starting from cholesterol and β- sitosterol.

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.

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