What is the Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)-?

Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)- is , while it's Molecular Formula is C 13 H 17 N. Used in Pharmaceutical Industry: Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)is used as a pharmaceutical intermediate for the synthesis of various pharmaceutical drugs. Its unique structure and chiral nature make it a valuable component in the development of new medications. Used in Neurological and Mood Disorder Treatment: Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)has potential applications in the treatment of neurological disorders and mood disorders due to its ability to interact with specific biological targets and modulate relevant signaling pathways. Used in Organic Synthesis: Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)is used as a building block in organic synthesis, enabling the creation of complex molecules and contributing to the advancement of chemical research and development. Used in Research and Industrial Settings: Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)is utilized in research and industrial settings for its unique properties and potential applications in various fields, including drug discovery, material science, and chemical engineering.

What is the CAS number for Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)-?

The CAS number of Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)- is 4528-51-2.

What is Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)- (4528-51-2) used for?

Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)-, also known as (S)-N-a-dimethyl-N-2-propynylbenzenemethanamine, is a chiral chemical compound with the molecular formula C11H15N. It is a single enantiomer with the (S)-configuration and is commonly used as a pharmaceutical intermediate. Benzeneethanamine, N,a-dimethyl-N-2-propynyl-, (S)plays a significant role in the synthesis of various pharmaceutical drugs and has potential applications in the treatment of neurological and mood disorders. Additionally, it serves as a building block in organic synthesis and is utilized in research and industrial settings.

Top Quality Chinese Factory supply 4528-51-2 Selegiline

Molecular Formula:C₁₃H₁₇N
Molecular Weight:187.285
PSA：3.24000
LogP:2.18260

4528-51-2 Relevant articles

Markovnikov Wacker-Tsuji Oxidation of Allyl(hetero)arenes and Application in a One-Pot Photo-Metal-Biocatalytic Approach to Enantioenriched Amines and Alcohols

Albarrán-Velo, Jesús,Gotor-Fernández, Vicente,Lavandera, Iván

supporting information, p. 4096 - 4108 (2021/08/19)

The Wacker-Tsuji aerobic oxidation of va...

Selegiline hydrochloride synthesis process

-

, (2020/01/25)

The invention relates to the field of ch...

Preparation method of selegiline

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Paragraph 0058; 0062-0065; 0069-0072; 0076-0078, (2019/08/14)

The invention provides a preparation met...

METHOD FOR PREPARING SELEGILINE BASE

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Paragraph 0040, (2018/08/12)

The present invention relates to a proce...

4528-51-2 Process route

: 33817-09-3
(R)-2-methylamino-1-phenylpropane

: 106-96-7
propargyl bromide

: 2323-36-6,4528-51-2,4530-70-5,14611-51-9
SELEGILINE

Conditions

Conditions	Yield
With tetrabutylammomium bromide; potassium carbonate; In water; toluene; for 24h; Ambient temperature;	82%
With potassium carbonate; In acetonitrile; at 25 ℃; for 12h;	72%
With potassium carbonate; In acetonitrile; at 25 ℃; for 3h;	71%
With potassium carbonate; In acetonitrile; at 50 ℃;	66.8%