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78261-67-3

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78261-67-3 Usage

Type of compound

Synthetic derivative of the hormone testosterone

Classification

Steroidal compound

Functional group

17β-carboxylic acid group

Biological activity

Potent androgen

Mechanism of action

Binds to and activates the androgen receptor

Potential use

Hormone replacement therapy

Target conditions

Testosterone deficiency and related conditions

Additional investigation

Performance-enhancing drug

Context of use

Athletic and bodybuilding pursuits

Check Digit Verification of cas no

The CAS Registry Mumber 78261-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,6 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78261-67:
(7*7)+(6*8)+(5*2)+(4*6)+(3*1)+(2*6)+(1*7)=153
153 % 10 = 3
So 78261-67-3 is a valid CAS Registry Number.

78261-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-3,11-dioxo-6,7,8,9 ,12,14,15,16-octahydrocyclopenta[a]phenanthrene-17-carboxylic aci d

1.2 Other means of identification

Product number -
Other names Medroxyprogesterone-caproate

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:78261-67-3 SDS

78261-67-3Upstream product

78261-67-3Downstream Products

78261-67-3Relevant articles and documents

Oxygen Atom Transfer from Iodylbenzene to Diphenyl Diselenide - A Convenient Method for Dehydrogenation of Steroidal 3-Ketones

Barton, Derek H. R.,Morzycki, Jacek W.,Motherwell, William B.,Ley, Steven V.

, p. 1044 - 1045 (2007/10/02)

Steroidal 3-ketones are smoothly dehydrogenated in high yield using benzeneseleninic anhydride generated in situ by oxygen atom transfer from iodylbenzene, PhIO2, to catalytic amounts of diphenyl diselenide; use of meta-iodylbenzoic acid in the above cycle has led to the development of an economical and experimentally convenient method avoiding chromatographic separations and with recovery of the m-iodobenzoic acid and the diphenyl diselenide.

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