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179328-22-4

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179328-22-4 Usage

General Description

N-Methyl-N-(4-morpholin-4-ylbenzyl)amine is a chemical compound that belongs to the class of organic compounds known as morpholines. It is an amine derivative that is commonly used as an intermediate in the synthesis of various pharmaceutical compounds. N-METHYL-N-(4-MORPHOLIN-4-YLBENZYL)AMINE has a molecular formula of C12H18N2O, and a molecular weight of 206.29 g/mol. It is a white to light yellow, crystalline solid at room temperature and is soluble in organic solvents such as methanol and ethanol. N-Methyl-N-(4-morpholin-4-ylbenzyl)amine is widely used in the production of anti-cancer drugs, antidepressants, and other therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 179328-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,3,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 179328-22:
(8*1)+(7*7)+(6*9)+(5*3)+(4*2)+(3*8)+(2*2)+(1*2)=164
164 % 10 = 4
So 179328-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2O/c1-13-10-11-2-4-12(5-3-11)14-6-8-15-9-7-14/h2-5,13H,6-10H2,1H3

179328-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-1-(4-morpholin-4-ylphenyl)methanamine

1.2 Other means of identification

Product number -
Other names N-methyl-N-(4-morpholin-4-ylbenzyl)amine

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:179328-22-4 SDS

179328-22-4Relevant articles and documents

Development and in Vitro Evaluation of a Microbicide Gel Formulation for a Novel Non-Nucleoside Reverse Transcriptase Inhibitor Belonging to the N-Dihydroalkyloxybenzyloxopyrimidines (N-DABOs) Family

Tintori, Cristina,Brai, Annalaura,Dasso Lang, Maria Chiara,Deodato, Davide,Greco, Antonia Michela,Bizzarri, Bruno Mattia,Cascone, Lorena,Casian, Alexandru,Zamperini, Claudio,Dreassi, Elena,Crespan, Emmanuele,Maga, Giovanni,Vanham, Guido,Ceresola, Elisa,Canducci, Filippo,Ari?n, Kevin K.,Botta, Maurizio

, p. 2747 - 2759 (2016/04/10)

Preventing HIV transmission by the use of a vaginal microbicide is a topic of considerable interest in the fight against AIDS. Both a potent anti-HIV agent and an efficient formulation are required to develop a successful microbicide. In this regard, molecules able to inhibit the HIV replication before the integration of the viral DNA into the genetic material of the host cells, such as entry inhibitors or reverse transcriptase inhibitors (RTIs), are ideal candidates for prevention purpose. Among RTIs, S- and N-dihydroalkyloxybenzyloxopyrimidines (S-DABOs and N-DABOs) are interesting compounds active at nanomolar concentration against wild type of RT and with a very interesting activity against RT mutations. Herein, novel N-DABOs were synthesized and tested as anti-HIV agents. Furthermore, their mode of binding was studied by molecular modeling. At the same time, a vaginal microbicide gel formulation was developed and tested for one of the most promising candidates.

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