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Benzenamine, 2,4,6-trichloro-N-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63333-26-6

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63333-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63333-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,3 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63333-26:
(7*6)+(6*3)+(5*3)+(4*3)+(3*3)+(2*2)+(1*6)=106
106 % 10 = 6
So 63333-26-6 is a valid CAS Registry Number.

63333-26-6SDS

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 2,4,6-trichloro-N-ethylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2,4,6-trichloro-N-ethyl

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:63333-26-6 SDS

63333-26-6Relevant academic research and scientific papers

Alkylarylamine compound and preparation method thereof

-

Paragraph 0044-0052, (2021/10/27)

The invention discloses an alkylarylamine compound and preparation method thereof. The preparation method mainly comprises the following steps: dissolving an alkyl compound, a nitro compound, an acid and a photocatalyst in a solvent; carrying out an illumination reaction at room temperature; after the reaction is finished, carrying out alkali neutralization, ethyl acetate extraction and reduced-pressure distillation to remove the solvent; and carrying out column chromatography separation to obtain the alkylarylamine compound. Compared with an alkylarylamine compound which has been widely researched and reported, the alkylarylamine compound provided by the invention has the advantages of simple operation, simple steps, high atom utilization rate, stable chemical properties, low cost, easy purification and the like; and since an alkyl group is directly activated, the method can realize conversion from low-added-value chemicals to high-added-value chemicals, and provides convenience for organic synthesis chemistry and drug synthesis.

A convenient preparation of N-alkyl and N-arylamines by smiles rearrangement - Synthesis of analogues of diclofenac

Wadia,Patil

, p. 2725 - 2736 (2007/10/03)

Smiles rearrangement of substituted aryloxyacetamides in which oxygen and nitrogen are separated by COCH2 group has been successful even when the aryloxy ring carries weak or no electron withdrawing group. Earlier reports of such reactions involved either strong electron withdrawing groups or a special catalyst. The diphenylamines thus obtained gave analogues of diclofenac in only one case.

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