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4062-46-8

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4062-46-8 Usage

Type

Synthetic androgen and anabolic steroid

Derivation

Derived from testosterone

Medical Uses

a. Treatment of low testosterone levels in men
b. Treatment of breast cancer in women
c. Stimulation of puberty in boys with delayed puberty
d. Hormone therapy for transgender men

Mechanism of Action

a. Increases the production of testosterone in the body (as an androgen)
b. Helps build and repair muscle tissue (as an anabolic steroid)

Side Effects

a. Liver toxicity
b. Masculinization in women
c. Mood changes

Precaution

Should only be used under the supervision of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 4062-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4062-46:
(6*4)+(5*0)+(4*6)+(3*2)+(2*4)+(1*6)=68
68 % 10 = 8
So 4062-46-8 is a valid CAS Registry Number.

4062-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,5S,8R,9S,10S,13S,14S,17S)-1,10,13-trimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] acetate

1.2 Other means of identification

Product number -
Other names (1|A,5|A,17|A)-1-methyl-3-oxoandrostan-17-yl 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:4062-46-8 SDS

4062-46-8Downstream Products

4062-46-8Relevant articles and documents

A CARBENOID ROUTE TO C(1)-C(11)BRIDGED STEROIDS

Kuenzer, H.,Bittler, D.,Rosenberg, D.,Sauer, G.,Wiechert, R.

, p. 6171 - 6174 (1990)

The exocyclic olefin 3 enters into stereoselective cyclopropanations with dihalocarbenes on the steroid β-face to afford the protected spirooctane analogues 4 and 5.These intermediates are transformed into novel, highly strained steroid derivatives, like 9, by utilizing an intramolecular cyclopropylidene insertion reaction en route to pentacyclic, C(1)-C(11)ethano-bridged steroids 13-20.

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