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2,1,3-Benzoxadiazol-4-amine, N-methyl-N-(1-methyl-2-phenylethyl)-7-nitrois a chemical compound characterized by a benzoxadiazole core and a nitro group. It is a derivative of N-methylamphetamine, a psychoactive drug. 2,1,3-Benzoxadiazol-4-amine,
N-methyl-N-(1-methyl-2-phenylethyl)-7-nitrois of interest in the fields of medicinal chemistry and drug discovery due to its unique structural features and properties, which may contribute to the development of new pharmaceuticals and biologically active molecules.

29902-39-4

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29902-39-4 Usage

Uses

Used in Medicinal Chemistry Research:
2,1,3-Benzoxadiazol-4-amine, N-methyl-N-(1-methyl-2-phenylethyl)-7-nitrois used as a research compound for exploring its potential in the development of new pharmaceuticals. Its unique structure and properties make it a valuable candidate for studying and creating novel drug molecules.
Used in Drug Discovery:
In the field of drug discovery, 2,1,3-Benzoxadiazol-4-amine, N-methyl-N-(1-methyl-2-phenylethyl)-7-nitrois utilized as a starting material or intermediate in the synthesis of new biologically active molecules. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, making it a key component in the search for innovative therapeutic agents.
Used in Material Science:
2,1,3-Benzoxadiazol-4-amine, N-methyl-N-(1-methyl-2-phenylethyl)-7-nitromay also find applications in material science, where its chemical properties could be harnessed to create new materials with unique characteristics. 2,1,3-Benzoxadiazol-4-amine,
N-methyl-N-(1-methyl-2-phenylethyl)-7-nitro-'s potential in this field is currently under investigation, with further research expected to reveal its full potential.
Used in Organic Synthesis:
In organic synthesis, 2,1,3-Benzoxadiazol-4-amine, N-methyl-N-(1-methyl-2-phenylethyl)-7-nitroserves as a versatile building block for the creation of complex organic molecules. Its reactivity and structural features make it a valuable component in the synthesis of a wide range of compounds, from pharmaceuticals to specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 29902-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,0 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29902-39:
(7*2)+(6*9)+(5*9)+(4*0)+(3*2)+(2*3)+(1*9)=134
134 % 10 = 4
So 29902-39-4 is a valid CAS Registry Number.

29902-39-4SDS

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 methyl-((S)-1-methyl-2-phenyl-ethyl)-(7-nitro-benzo[1,2,5]oxadiazol-4-yl)-amine

1.2 Other means of identification

Product number -
Other names N-<4-Nitro-benzo-2-oxa-1,3-diazolyl-(7)>-methamphetamin

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:29902-39-4 SDS

29902-39-4Downstream Products

29902-39-4Relevant academic research and scientific papers

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