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7-ketopregnenolone acetate is a chemical compound derived from pregnenolone, a hormone produced in the adrenal glands and gonads. It is a steroidal ketone with a molecular formula of C21H30O3 and a molecular weight of 330.46 g/mol. 7-ketopregnenolone acetate is characterized by the presence of a ketone group at the 7-position and an acetate group attached to the 3-hydroxyl group. 7-ketopregnenolone acetate plays a role in the synthesis of various steroid hormones and has been studied for its potential effects on the nervous system and cognitive function. It is also used as an intermediate in the production of other steroidal compounds. Due to its complex structure and potential applications, 7-ketopregnenolone acetate is a subject of interest in the fields of chemistry, pharmacology, and endocrinology.

6748-09-0

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6748-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6748-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6748-09:
(6*6)+(5*7)+(4*4)+(3*8)+(2*0)+(1*9)=120
120 % 10 = 0
So 6748-09-0 is a valid CAS Registry Number.

6748-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-acetyloxy-3β-pregn-5-en-7,20-dione

1.2 Other means of identification

Product number -
Other names 7-ketopregnenolone acetate

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:6748-09-0 SDS

6748-09-0Upstream product

6748-09-0Relevant academic research and scientific papers

Highly stereoselective epoxidation with H2O2 catalyzed by electron-rich aminopyridine manganese catalysts

Cusso, Olaf,Garcia-Bosch, Isaac,Font, David,Ribas, Xavi,Lloret-Fillol, Julio,Costas, Miquel

supporting information, p. 6158 - 6161 (2014/01/17)

Fast, efficient, and highly stereoselective epoxidation with H 2O2 is reached by manganese coordination complexes with e-rich aminopyridine tetradentate ligands. It is shown that the electronic properties of these catalysts vary systematically with the stereoselectivity of the O-atom transfer event and exert fine control over the activation of hydrogen peroxide, reducing the amount of carboxylic acid co-catalyst necessary for efficient operation.

Epalons: 6-substituted derivatives of 7-norepiallopregnanolone

Kasal, Alexander

, p. 3559 - 3565 (2007/10/03)

The target compounds (3α-hydroxy-5,6-epoxy-7-nor-5α-pregnan-20-one, 3α-hydroxy-5,6β-epoxy-7-nor-5β-pregnan-20-one and 3α-hydroxy-7-nor-5α- pregnane-6,20-dione) were prepared from 5,6β-dihydroxy-20-oxo-5α-pregnan- 3β-yl acetate via the corresponding 5,6-se

Stereoselective 7α-hydroxylation of 3β-acetoxy-Δ5-steroids by Fe(PA)3/H2O2/MeCN

Kotani, Eiichi,Takeya, Tetsuya,Egawa, Hirotaka,Tobinaga, Seisho

, p. 750 - 752 (2007/10/03)

Stereoselective 7α-hydroxylation reaction of Δ5-steroids by a Fe(PA; picolinate)3/H2O2/MeCN system is presented. The 7α-hydroxylation reactions were achieved in 33-40% yields by addition of 30%-H2O2 to a solution of 3β-acetoxy-Δ5-steroids 1a-1d and a crystalline of Fe(PA)3 in MeCN.

Benzotriazole-Chromium Trioxide Complex a Versatile Oxidant of Organic Compounds

Parish, Edward J.,Honda, Hiroshi,Hileman, Deborah L.

, p. 3359 - 3366 (2007/10/02)

Benzotriazole has been found to complex with chromium trioxide to produce a versatile new oxidant.This complex is capable of oxidizing primary alcohols to carboxylic acids, secondary alcohols to ketones, and bringing about the allylic oxidation of olefin substrates.

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