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1246172-66-6

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1246172-66-6 Usage

Main Properties

1. Chemical Name: 2-Amino-N-ethyl-3-phenylpropanamide hydrochloride
2. Alias: Norethandrolone
3. Classification: Synthetic anabolic steroid
4. Derivative: Derived from testosterone
5. Medical Usage: Hormone-related disorder treatment and muscle mass increase in specific medical conditions
6. Salt Form: Hydrochloride salt
7. Solubility: Enhanced solubility and stability in aqueous solution
8. Pharmaceutical Suitability: Suitable for pharmaceutical formulations
9. Mechanism of Action: Binds to and activates the androgen receptor
10. Effects: Increase in protein synthesis and muscle growth
11. Regulation: Controlled substance due to abuse and misuse potential

Chemical Structure

2-Amino-N-ethyl-3-phenylpropanamide

Functionality

Androgenic and anabolic properties

Medical Applications

Treatment of hormone-related disorders such as hypogonadism and muscle wasting conditions

Route of Administration

Typically administered orally

Dosage Forms

Available in various forms including tablets and injections

Legal Status

Subject to regulation and control by authorities due to its potential for misuse and abuse

Side Effects

Potential adverse effects include liver toxicity, cardiovascular issues, and hormonal imbalances

Detection

Can be detected in drug tests for athletic competitions and other purposes

Interactions

May interact with other medications and substances, leading to adverse effects or altered efficacy

Monitoring

Requires careful monitoring during usage to manage potential risks and ensure therapeutic benefits

This comprehensive list covers the main properties and specific content of 2-Amino-N-ethyl-3-phenylpropanamide hydrochloride, also known as Norethandrolone.

Check Digit Verification of cas no

The CAS Registry Mumber 1246172-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,1,7 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1246172-66:
(9*1)+(8*2)+(7*4)+(6*6)+(5*1)+(4*7)+(3*2)+(2*6)+(1*6)=146
146 % 10 = 6
So 1246172-66-6 is a valid CAS Registry Number.

1246172-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-N-ethyl-3-phenylpropanamide hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:1246172-66-6 SDS

1246172-66-6Relevant articles and documents

Direct joining of a heterogeneous pair of supramolecular nanotubes and reaction control of a guest compound by transportation in the nanochannels

Kameta, Naohiro,Ding, Wuxiao

, p. 1053 - 1059 (2019/07/19)

Four novel amino-acid lipids were synthesized and then self-assembled in water to produce four different types of supramolecular nanotubes. The nanotubes consisted of a single monolayer of amino-acid lipids packed in parallel and had similar inner diameters and membrane wall thicknesses but dissimilarly charged surfaces. Mixing of nanotubes that had cationic exterior surfaces with nanotubes that had anionic exterior surfaces resulted in aggregation of the nanotubes. In contrast, mixing of nanotubes with cationic interior surfaces and nanotubes with anionic interior surfaces resulted in end-to-end joining of the two types of nanotubes via electrostatic attractions at the open ends to form heterogeneous nanotubes. Time-lapse fluorescence microscopy confirmed that a fluorophore could be transported through the heterogeneous nanotubes, which had alternating acidic and basic nanochannel segments. In addition, acidbase reactions of the fluorophore could be precisely controlled during transport. This nanotube-joining technique should be useful not only for the construction of multifunctional hybrid nanotubes but also for the production of nanoreactors for chemical/biological reactions and nano-devices for analysis and separation.

Studies on analgesic oligopeptides. V. Structure-activity relationship of tripeptide alkylamides, Tyr-D-Arg-Phe-X

Suzuki,Fujita,Sasaki,Shiratori,Sakurada,Kisara

, p. 4834 - 4840 (2007/10/02)

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