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Acetate ester of 20-oxopregnan-3-ol found in the adrenal cortex

2394-44-7

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2394-44-7 Usage

Chemical compound

20-oxopregnan-3-yl acetate

Family

Pregnan steroid

Function

Regulating stress and immune function

Use as a biomarker

Potential for certain diseases and conditions

Potential applications

Pharmaceuticals and as a precursor for synthesis of bioactive compounds

Promise for medical and research fields

Various applications for 20-oxopregnan-3-yl acetate in both fields

Check Digit Verification of cas no

The CAS Registry Mumber 2394-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2394-44:
(6*2)+(5*3)+(4*9)+(3*4)+(2*4)+(1*4)=87
87 % 10 = 7
So 2394-44-7 is a valid CAS Registry Number.

2394-44-7SDS

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 Pregnan-3.β.-ol-20-one acetate

1.2 Other means of identification

Product number -
Other names epipregnanolone 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:2394-44-7 SDS

2394-44-7Relevant academic research and scientific papers

HELIX 12 DIRECTED STEROIDAL PHARMACEUTICAL PRODUCTS

-

Page/Page column 139, (2010/02/12)

Compounds having the structure or their salts: are used to treat or reduce le likelihood of acquiring androgen-dependent diseases, such as prostate cancer, benign prostatic hyperplasia, polycystic ovarian syndrome, acne, hirsutism, seborrhea, androgenic alopecia and male baldness. They can be formulated together with pharmaceutically acceptable diluent or carrier or otherwise made into any pharmaceutical dosage form. Some of these compounds having tissue-specific antiandrogenic activity and tissue-specific androgenic activity can be used to treat or reduce the risk of developing diseases related to loss of androgenic stimulation. Combinations with other active pharmaceutical agents are also disclosed.

PYRIDINIUM DICHROMATE IN ORGANIC SYNTHESIS: A CONVENIENT OXIDATION OF α-YNOL-IODINE COMPLEXES TO α,β-UNSATURATED-α-IODO-ALDEHYDES

Antoniolett, R.,D'Auria, M.,Piancatelli, G.,Scettri, A.

, p. 1041 - 1042 (2007/10/02)

Under mild and simple conditions PDC oxidizes α-ynol-I2 complexes to the title carbonyl compounds.

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