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418784-70-0

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418784-70-0 Usage

Description

1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine is a chemical compound with the molecular formula C15H16N2O3. It is a derivative of methanamine and contains a 4-methoxyphenyl group and a 4-nitrobenzyl group. 1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine is known for its potential biological activities and pharmacological properties, making it a valuable asset in research and pharmaceutical applications. Its specific characteristics and uses will depend on the intended application and the context in which it is utilized.

Uses

Used in Pharmaceutical Applications:
1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine is used as an active pharmaceutical ingredient for its potential therapeutic effects. 1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Research and Development:
In the research industry, 1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine is used as a key compound for studying its biological activities and pharmacological properties. This helps scientists understand its potential applications in medicine and drug development.
Used in Organic Synthesis:
1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine also serves as a building block for the synthesis of other organic compounds. Its unique structure makes it a valuable component in the creation of new molecules with specific properties and applications.
Used in Chemical Analysis:
1-(4-methoxyphenyl)-N-(4-nitrobenzyl)methanamine can be employed in chemical analysis to study its interactions with various reagents and conditions. This information can be used to optimize its synthesis and application in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 418784-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,8,7,8 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 418784-70:
(8*4)+(7*1)+(6*8)+(5*7)+(4*8)+(3*4)+(2*7)+(1*0)=180
180 % 10 = 0
So 418784-70-0 is a valid CAS Registry Number.

418784-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-methoxyphenyl)methyl]-1-(4-nitrophenyl)methanamine

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:418784-70-0 SDS

418784-70-0Downstream Products

418784-70-0Relevant articles and documents

Cs2CO3-Promoted Direct N-Alkylation: Highly Chemoselective Synthesis of N-Alkylated Benzylamines and Anilines

Castillo, Juan-Carlos,Orrego-Hernández, Jessica,Portilla, Jaime

, p. 3824 - 3835 (2016/08/20)

Herein is described an efficient and chemoselective method for the synthesis of diversely substituted secondary amines in yields up to 98 %. Direct mono-N-alkylation of primary benzylamines and anilines with a wide range of alkyl halides is promoted by a cesium base in the absence of any additive or catalyst. The basicity and solubility of cesium carbonate in anhydrous N,N-dimethylformamide not only enables mono-N-alkylation of primary amines but also suppresses undesired dialkylation of the desired amines.

1,2,3-Triazole-boranes: Stable and efficient reagents for ketone and aldehyde reductive amination in organic solvents or in water

Liao, Wenyan,Chen, Yunfeng,Liu, Yuxiu,Duan, Haifeng,Petersen, Jeffrey L.,Shi, Xiaodong

supporting information; experimental part, p. 6436 - 6438 (2010/03/04)

Air, moisture and thermally stable 1,2,3-triazole-borane complexes were developed as new practical reagents for ketone/aldehyde amination with high efficiency and excellent substrate diversity.

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