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Benzenamine, 2-(1,3-dioxolan-2-yl)-4-methoxy-, also known as 2-(1,3-dioxolan-2-yl)-4-methoxyaniline, is an organic compound with the chemical formula C10H13NO3. It is a derivative of aniline, featuring a 1,3-dioxolane ring and a methoxy group attached to the benzene ring. Benzenamine, 2-(1,3-dioxolan-2-yl)-4-methoxy- is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its molecular structure provides unique reactivity and selectivity, making it a valuable building block in organic synthesis. The compound is typically synthesized through various chemical reactions, such as the condensation of aniline with a suitable aldehyde or ketone in the presence of a catalyst. Due to its potential applications in the production of active ingredients, it is important to handle Benzenamine, 2-(1,3-dioxolan-2-yl)-4-methoxy- with care, following proper safety protocols.

64389-34-0

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64389-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64389-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,8 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64389-34:
(7*6)+(6*4)+(5*3)+(4*8)+(3*9)+(2*3)+(1*4)=150
150 % 10 = 0
So 64389-34-0 is a valid CAS Registry Number.

64389-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-dioxolan-2-yl)-4-methoxyaniline

1.2 Other means of identification

Product number -
Other names 5-methoxy-2-aminobenzaldehyde ethylene acetal

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:64389-34-0 SDS

64389-34-0Relevant academic research and scientific papers

BIARYLTRIAZOLE INHIBITORS OF MACROPHAGE MIGRATION INHIBITORY FACTOR

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Page/Page column 187, (2016/09/22)

The present disclosure describes biaryl triazole compounds, as well as their compositions and methods of use. The compounds inhibit the activity of macrophage migration inhibitory factor and are useful for the treatment of diseases, e.g., inflammatory dis

Heterobicyclic sphingosine 1-phosphate analogs

-

Page/Page column, (2014/04/18)

Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.

Design and synthesis of 6,6-fused heterocyclic amides as raf kinase inhibitors

Ramurthy, Savithri,Costales, Abran,Jansen, Johanna M.,Levine, Barry,Renhowe, Paul A.,Shafer, Cynthia M.,Subramanian, Sharadha

supporting information; experimental part, p. 1678 - 1681 (2012/04/04)

Compounds belonging to several scaffolds-quinazolines, quinolines and quinoxalines-were designed and synthesized as Raf kinase inhibitors. Scaffolds were assessed for in vitro BrafV600E inhibition, and overall kinase selectivity. Pharmacokinetic parameters for one of the scaffolds were also determined.

HETEROBICYCLIC SPHINGOSINE 1-PHOSPHATE ANALOGS

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Page/Page column 46, (2010/05/14)

Compounds that have agonist activity at one or more of the SlP receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at SlP receptors.

2,6-Disubstituted quinazolines, quinoxalines, quinolines and isoquinolines and methods of their use as inhibitors of RAF kinase

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Page/Page column 14; 17, (2010/02/11)

New substituted quinazoline, quinoxaline, quinoline and isoquinoline compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

Plant antitumor agents: Synthesis and biological activity of camptothecin analogues

Wani,Ronman,Lindley,Wall

, p. 554 - 560 (2007/10/02)

Four analogues, 10-methoxy (20), 12-aza (29), benz[j] (36), and 18-methoxy (38), of camptothecin were obtained by total synthesis. The two water-soluble analogues, 10-[(carboxymethyl)oxy] (24) and 10-[2'-(diethylamino)-ethoxy]-20(S)-camptothecin (26), wit

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