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(2E)-3-[(4-bromo-3-methylphenyl)amino]-1-(4-methylphenyl)prop-2-en-1-one is a complex organic compound characterized by its unique molecular structure. It features a 2-en-1-one backbone, which is a type of enone, with a double bond between the second and third carbon atoms. The compound is further defined by the presence of a 4-bromo-3-methylphenyl group attached to the nitrogen atom of the enamine, and a 4-methylphenyl group attached to the carbonyl carbon. This specific arrangement of functional groups and substituents gives the molecule distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

6085-15-0

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6085-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6085-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6085-15:
(6*6)+(5*0)+(4*8)+(3*5)+(2*1)+(1*5)=90
90 % 10 = 0
So 6085-15-0 is a valid CAS Registry Number.

6085-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-bromo-3-methylanilino)-1-(4-methylphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names ethyl 2,3,3-triethoxybutanoate

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:6085-15-0 SDS

6085-15-0Downstream Products

6085-15-0Relevant academic research and scientific papers

Catalytic Role of Copper Triflate in Lewis Acid Promoted Reactions of Diazo Compounds

Doyle, Michael P.,Trudell, Mark L.

, p. 1196 - 1199 (2007/10/02)

Copper(II)trifluoromethanesulfonate is often a superior catalyst for transformations of diazo compounds that are normally promoted by boron trifluoride etherate.Formal carbon-oxygen insertion occurs when ortho esters are reacted with diazocarbonyl compounds in the presence of Cu(OTf)2, although the use of BF3*Et2O provides higher yields of insertion products.In contrast, the β,γ-unsaturated diazo ketone 6 undergoes intramolecular cyclization to produce the corresponding cyclopentenone in higher yield with Cu(OTf)2 catalysis than with the use of BF3*Et2O.Intamolecular cyclopropanation of the γ,δ-unsaturated diazo ketone 8 occurs in exceptionally high yield in the presence of Cu(OTf)2, whereas with BF3*Et2O intramolecular cyclization occurs with extensive rearrangement anf fluoride transfer.Copper(II)triflate is unique among transition-metal catalysts that are normally employed for reactions with diazo compounds in its effectiveness for these transformations.

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