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Androst-4-ene-3,17-dione, also known as 4-Androstene-3,17-dione or 4-Androstene-3,17-dione, is a steroidal compound with the chemical formula C19H26O2. It is a derivative of androstenedione, featuring a double bond at the 4th carbon and a ketone group at both the 3rd and 17th carbons. Androst-4-ene-3,17-dione,(9â,10R)- is an important intermediate in the synthesis of various steroidal drugs and hormones, such as testosterone and other anabolic steroids. It is also used in the pharmaceutical industry for the production of contraceptives and other hormone-related medications. The (9α,10R)- configuration refers to the specific stereochemistry of the molecule, which is crucial for its biological activity and interactions within the body.

571-45-9

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571-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 571-45-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 571-45:
(5*5)+(4*7)+(3*1)+(2*4)+(1*5)=69
69 % 10 = 9
So 571-45-9 is a valid CAS Registry Number.

571-45-9SDS

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 (9β,10α)-androst-4-ene-3,17-dione

1.2 Other means of identification

Product number -
Other names 9β,10α-Androst-4-en-3,17-dion

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:571-45-9 SDS

571-45-9Relevant academic research and scientific papers

Platinum-Catalyzed α,β-Desaturation of Cyclic Ketones through Direct Metal–Enolate Formation

Chen, Ming,Dong, Guangbin

supporting information, p. 7956 - 7961 (2021/03/01)

The development of a platinum-catalyzed desaturation of cyclic ketones to their conjugated α,β-unsaturated counterparts is reported in this full article. A unique diene-platinum complex was identified to be an efficient catalyst, which enables direct metal-enolate formation. The reaction operates under mild conditions without using strong bases or acids. Good to excellent yields can be achieved for diverse and complex scaffolds. A wide range of functional groups, including those sensitive to acids, bases/nucleophiles, or palladium species, are tolerated, which represents a distinct feature from other known desaturation methods. Mechanistically, this platinum catalysis exhibits a fast and reversible α-deprotonation followed by a rate-determining β-hydrogen elimination process, which is different from the prior Pd-catalyzed desaturation method. Promising preliminary enantioselective desaturation using a chiral-diene-platinum complex has also been obtained.

A FACILE SYNTHESIS OF STEROIDAL Δ4-3-KETONES USING PYRIDINIUM CHLOROCHROMATE (PCC)

Parish, Edward J.,Honda, Hiroshi

, p. 1167 - 1174 (2007/10/02)

Pyridinium chlorochromate (PCC), in refluxing benzene, has been found to be an affective and convenient reagent for the oxidation and concomitant isomerization of steroidal Δ5-3β-alcohols to the corresponding Δ4-3-ketones in high yield.

SELECTIVITE DE LA REDUCTION D'α-ENONES POLYCYCLIQUES PAR LES BOROHYDRURES: EFFET DE L'ADDITION DE TETRAMETHYL-ETHYLENEDIAMINE AU BOROHYDRURE DE TETRABUTYLAMMONIUM

D'incan, E.,Loupy, A.,Maia, A.,Seyden-Penne, J.,Viout, P.

, p. 2923 - 2927 (2007/10/02)

Δ1,9octalone, Δ1,9-10-methyl octalone and testosterone were reduced by NBu4BH4, alone or in the presence of tetramethylethylenediamine (TMEDA), in THF and in toluene.With TMEDA, the first step of the reduction is the regioselective 1,4 attack by BH4(1-) which leads either to the saturated ketones or to the corresponding saturated alcohols.The results observed under different conditions were interpreted by the intervention of various reductive species: diborane, enoxyborohydrides in the absence of TMEDA, amine-borane in its presence.

Formation of vinyl halides from vinyl cations generated by acetylenic participation in biomimetic polyene cyclizations

Johnson, William S.,Ward, Carl E.,Boots, Sharon G.,Gravestock, Michael B.,Markezich, Ronald L.,McCarry, Brian E.,Okorie, Dominic A.,Parry, Ronald J.

, p. 88 - 98 (2007/10/02)

The object of this study was to examine the fate of vinyl cations of type 4 (resulting from biomimetic polyene cyclizations) in the presence of various halides as sources of nucleophiles. Treatment of the dienynol 1 with trifluoroacetic acid in methylene chloride for 45 min at -78°C resulted in the isolation of the rearranged bicyclic vinyl chloride 6 in 56% yield. Confirmation of the structure and isomeric purity of 6 was obtained by exhaustive ozonization to give diketo ester 9 followed by Wolff-Kischner reduction and then esterification to yield ester 10, the structure of which was confirmed by hydrogen-deuterium exchange of the protons α to the carbomethoxy group. The configuration of the ring fusion in 6 was shown to be trans in the following manner. Selective ozonization gave chloro ketone 11, which was converted into chloro olefin 12 by Wolff-Kischner reduction. Further ozonization afforded keto ester 13, which was converted into diacid 15 by sodium hypobromite oxidation. Esterification afforded diester 16, which was identical with the material obtained via Wolff-Kischner reduction of the known keto diester 17. More careful examination of the products from the aforementioned cyclization also showed the presence of 8% ketone 8 (after hydrolytic workup). Identical cyclization conditions of 1, except at 0°C, gave 55% vinyl chloride 6 and 45% ketone 8 while use of a 7.5:1 pentane-1,2-dichloroethane mixture at 0°C led to 11% vinyl chloride 6 and 89% ketone 8. Cyclization of dienynol 1 with stannic chloride in 1,1-dichloroethylene at -35°C for 45 min gave a 53% yield of three isomeric vinyl chlorides, 7b, 7a, and 6, in a ratio of 8:75:12. The successful cyclization of dienynol 1 led to more extensive cyclization studies of substrates such as 2, 3, and 35, which provided tetracyclic products. The most thoroughly studied case was that of trienynol 3, which, on treatment with stannic chloride in 1,1-dichloroethylene at ca. -30°C for 50 min, gave a 64% yield of three tetracyclic products A, B, and C in a ratio of 15:73:12 by VPC. Product A was shown to be chloro diene 22 by hydrogenation of the Δ1-olefinic bond followed by ozonization to give 5β,13α-androstan-17-one (29), which was compared with an authentic sample prepared by irradiation of 5β-androstan-17-one (25). Products B and C were shown to be chloro dienes 18 and 20 by conversion of the mixture into 5β-androstan-17-one (25) and keto ester 27. A systematic variation of reaction conditions as well as the use of mixed-halide sources led to evidence for a possible mechanism for the formation of all three products from an intermediary tricyclic cation 43.

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