Welcome to LookChem.com Sign In|Join Free

CAS

  • or

846-46-8

Post Buying Request

846-46-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

846-46-8 Usage

Uses

5α-Androstanedione is a metabolite of Androstendione (A637550). 5α-Androstanedione is an important intermediate in the conversion of Androstenedione to Androstanolone (A637540).

Definition

ChEBI: The 5alpha-stereoisomer of androstane-3,17-dione.

Check Digit Verification of cas no

The CAS Registry Mumber 846-46-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 846-46:
(5*8)+(4*4)+(3*6)+(2*4)+(1*6)=88
88 % 10 = 8
So 846-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-16H,3-11H2,1-2H3/t12-,14?,15?,16?,18?,19?/m0/s1

846-46-8SDS

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 5α-androstane-3,17-dione

1.2 Other means of identification

Product number -
Other names Boldenone Undecanoate

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:846-46-8 SDS

846-46-8Relevant articles and documents

Miescher,Wettstein

, p. 112,116 (1939)

Kinetic analysis of androstenedione 5α-reductase in epithelium and stroma of human prostate

Weisser, Heike,Krieg, Michael

, p. 589 - 594 (1997)

In the human prostate, various androgen-metabolizing enzymes are present. Among these enzymes, testosterone 5α-reductase seems to be dominant. However androstenedione is also a potential substrate of the prostatic 5α-reductase. To address the question of to what extent the reduction of androstenedione to androstanedione occurs, the present study describes in detail the kinetic characteristics (K(m) and V(max)) and possible age-dependent alterations of this enzymatic step in epithelium and stroma of the human prostate. In normal prostate (NPR), the mean K(m) (nM) and V(max) (pmol/mg protein · h) were about twofold higher in stroma (K(m) 211; V(max), 130) than in epithelium (K(m), 120; V(max), 56), whereas in the benign prostatic hyperplasia (BPH), the mean K(m) (nM; mean ± SEM) and V(max) (pmol/mg protein · h: mean ± SEM) were about sixfold higher in stroma (K(m), 688 ± 121; V(max), 415 ± 73) than in epithelium (K(m), 120 ± 10; V(max), 73 ± 8). In BPH, those differences between epithelium and stroma were highly significant (p 0.001). However, the efficiency ratios (V(max)/K(m)) of neither BPH nor NPR showed any significant differences between epithelium (NPR, 0.47; BPH, 0.62 ± 0.06) and stroma (NPR, 0.70; BPH. 0.63 ± 0.05). With respect to age-related changes, only stroma showed a significant increase of K(m) (P 0.01) and V(max) (p 0.05) with age. In summary, in both epithelium and stroma of the human prostate, a 5α-reductase converts in measurable amounts androstenedione to androstanedione. The kinetic data were, in part, different between epithelium and stroma; the reason for this difference remains unclear. In comparison to other metabolic conversions, such as testosterone to dihydrotestosterone and androstenedione to testosterone, it is unlikely that, in the human prostate, the adrenal androgen androstenedione contributes significantly to the formation of testosterone and, further, of dihydrotestosterone.

A sodium trifluoromethanesulfinate-mediated photocatalytic strategy for aerobic oxidation of alcohols

Zhu, Xianjin,Liu, Can,Liu, Yong,Yang, Haijun,Fu, Hua

, p. 12443 - 12446 (2020/10/30)

A sodium trifluoromethanesulfinate-mediated photocatalytic strategy for the aerobic oxidation of alcohols has been developed for the first time, and the photoredox aerobic oxidation of secondary and primary alcohols provided the corresponding ketones and carboxylic acids, respectively, in high to excellent yields.

Preparation method 5α- androstane -3,17- diketone (by machine translation)

-

, (2020/03/17)

The preparation method 5α - of, androstane - 333317-dione comprises the following steps: (4 -) preparing the compound, androstanone through 17-hydroxycyanidation, 3-hydroxycyanidation- 17-hydroxycyanidation of, 5,6-hydroxycyanidation to, 3-position ketal acid hydrolysis as the raw material 5α - and the method has the advantages. of low production cost, product purity. (by machine translation)

Photochemical Transformations with Iodine Azide after Release from an Ion-Exchange Resin

Dr?ger, Gerald,K?sel, Teresa,Kirschning, Andreas,Schulz, G?ran

supporting information, p. 12376 - 12380 (2020/05/08)

This report discloses the photochemical homolytic cleavage of iodine azide after its formation following release from polymer-bound bisazido iodate(I) anions. A series of radical reactions are reported including the 1,2-functionlization of alkenes and the unprecedented chemoselective oxidation of secondary alcohols in the presence of primary alcohols.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 846-46-8