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Benzenamine, 2-methoxy-N-(4-nitrophenyl)-, also known as 2-methoxy-4'-nitro-diphenylamine or 2-methoxy-4-nitroaniline, is an organic compound with the chemical formula C13H12N2O3. It is a derivative of aniline, featuring a methoxy group at the 2-position and a 4-nitrophenyl group attached to the nitrogen atom. This yellow crystalline solid is used as a chemical intermediate in the synthesis of various dyes, pharmaceuticals, and other organic compounds. Due to its reactivity and potential health hazards, it is important to handle Benzenamine, 2-methoxy-N-(4-nitrophenyl)- with care, following proper safety protocols.

729-04-4

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729-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729-04-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 729-04:
(5*7)+(4*2)+(3*9)+(2*0)+(1*4)=74
74 % 10 = 4
So 729-04-4 is a valid CAS Registry Number.

729-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-N-(4-nitrophenyl)aniline

1.2 Other means of identification

Product number -
Other names 2-methoxy-4'-nitrodiphenylamine

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:729-04-4 SDS

729-04-4Relevant academic research and scientific papers

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

Akram, Manjur O.,Das, Avishek,Chakrabarty, Indradweep,Patil, Nitin T.

supporting information, p. 8101 - 8105 (2019/10/11)

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.

SAR and lead optimization of an HIV-1 Vif-APOBEC3G axis inhibitor

Mohammed, Idrees,Parai, Maloy K.,Jiang, Xinpeng,Sharova, Natalia,Singh, Gatikrushna,Stevenson, Mario,Rana, Tariq M.

, p. 465 - 469 (2012/09/22)

We describe structure-activity relationship and optimization studies of RN-18, an HIV-1 Vif-APOBEC3G axis inhibitor. Targeted modifications of RN-18 ring C, ring B, ring A, bridge A-B, and bridge B-C were performed to identify the crucial structural features, which generated new inhibitors with similar (4g and 4i) and improved (5, 8b, and 11) activities. Two potent water-soluble RN-18 analogues, 17 and 19, are also disclosed, and we describe the results of pharmacological studies with compound 19. The findings described here will be useful in the development of more potent Vif inhibitors and in the design of probes to identify the target protein of RN-18 and its analogues.

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