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4-Propyloxybenzylamine, with the molecular formula C10H15NO, is an amine derivative characterized by the attachment of a propyloxy group to the benzylamine structure. It is a versatile chemical compound that plays a significant role in various chemical and pharmaceutical research applications.

21244-33-7

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21244-33-7 Usage

Uses

Used in Organic Synthesis:
4-Propyloxybenzylamine is used as a building block in organic synthesis for the preparation of various pharmaceutical and biologically active compounds. Its unique structure allows for the creation of diverse molecules with potential applications in medicine and other fields.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-Propyloxybenzylamine serves as a key component in the development of novel drugs. Its ability to be incorporated into complex molecular structures makes it valuable for designing new therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Development:
4-Propyloxybenzylamine also finds application in the agrochemical industry, where it is utilized in the synthesis of new agrochemicals. Its potential to be part of active ingredients in pesticides or fertilizers contributes to the development of more effective and environmentally friendly products.
Used in Materials Science:
In the field of materials science, 4-Propyloxybenzylamine has potential applications in the synthesis of functionalized polymers and materials with specific properties. Its incorporation into these materials can lead to the development of advanced materials with tailored characteristics for various applications.
Overall, 4-Propyloxybenzylamine is a multifaceted compound with a wide range of applications across different industries, including pharmaceuticals, agrochemicals, and materials science, due to its unique structure and versatility in synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 21244-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,4 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21244-33:
(7*2)+(6*1)+(5*2)+(4*4)+(3*4)+(2*3)+(1*3)=67
67 % 10 = 7
So 21244-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-2-7-12-10-5-3-9(8-11)4-6-10/h3-6H,2,7-8,11H2,1H3

21244-33-7SDS

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 (4-Propoxybenzyl)amine

1.2 Other means of identification

Product number -
Other names (4-propoxyphenyl)methanamine

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:21244-33-7 SDS

21244-33-7Relevant academic research and scientific papers

COMPOUNDS, SALTS THEREOF AND METHODS FOR TREATMENT OF DISEASES

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Paragraph 00677-00678, (2019/03/12)

The present disclosure relates to compounds according to Formula (I), useful for treating diseases.

Tuneable hydrogenation of nitriles into imines or amines with a ruthenium pincer complex under mild conditions

Choi, Jong-Hoo,Prechtl, Martin H. G.

, p. 1023 - 1028 (2015/03/18)

The selective hydrogenation of aromatic and aliphatic nitriles into amines and imines is described. Using a ruthenium pincer complex, the selectivity towards amines or imines can be controlled by simple parameter changes. The reactions are conducted under very mild conditions between 50-100°C at 0.4 MPa H2 pressure without any additives at low catalytic loadings of 0.5-1 mol %, which results in quantitative conversions and high selectivity.

Carnosine analogues containing NO-donor substructures: Synthesis, physico-chemical characterization and preliminary pharmacological profile

Bertinaria, Massimo,Rolando, Barbara,Giorgis, Marta,Montanaro, Gabriele,Marini, Elisabetta,Collino, Massimo,Benetti, Elisa,Daniele, Pier Giuseppe,Fruttero, Roberta,Gasco, Alberto

experimental part, p. 103 - 112 (2012/08/29)

The synthesis, physico-chemical, and biological characterisation of a short series of carnosine amides bearing NO-donor nitrooxy functionalities are described. The NO-donor carnosine analogues and their des-NO derivatives display carnosine-like properties

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