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Androst-4-ene-3-one-17-ethylene ketal is a synthetic chemical compound derived from androst-4-ene-3-one, a naturally occurring steroid. androst-4-ene-3-one-17-ethylene ketal is characterized by the presence of a ketal functional group at the 17th carbon position, which is formed by the reaction of the ketone group with ethylene oxide. It is often used in the synthesis of various pharmaceuticals and other chemical products due to its unique structure and reactivity. The compound plays a significant role in the development of new drugs and has potential applications in the fields of medicine and chemistry.

1044-89-9

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1044-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1044-89-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1044-89:
(6*1)+(5*0)+(4*4)+(3*4)+(2*8)+(1*9)=59
59 % 10 = 9
So 1044-89-9 is a valid CAS Registry Number.

1044-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name androst-4-ene-3-one-17-ethylene ketal

1.2 Other means of identification

Product number -
Other names 17-ethylendioxyandrost-4-en-3-one

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:1044-89-9 SDS

1044-89-9Relevant academic research and scientific papers

Cleavage of acetals promoted by copper (II) sulphate adsorbed on silica gel

Cabellero,Gros

, p. 395 - 404 (2007/10/02)

Copper sulphate supported on silica gel promotes the easy removal of cyclic acetals and tetrahydropyranyl ethers to give the respective parent carbonyl and hydroxyl compounds.

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