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2-Propen-1-one, 1-(5-bromo-2-hydroxyphenyl)-3-phenyl-3-[(phenylmethyl)amino]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109619-17-2

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109619-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109619-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,6,1 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109619-17:
(8*1)+(7*0)+(6*9)+(5*6)+(4*1)+(3*9)+(2*1)+(1*7)=132
132 % 10 = 2
So 109619-17-2 is a valid CAS Registry Number.

109619-17-2SDS

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 (Z)-3-(benzylamino)-1-(5-bromo-2-hydroxyphenyl)-3-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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:109619-17-2 SDS

109619-17-2Downstream Products

109619-17-2Relevant academic research and scientific papers

REACTIONS OF 3-ARYL-1--2-PROPYN-1-ONES IN THE PRESENCE OF AMINES. TWO TYPES OF INTRAMOLECULAR CYCLIZATION INVOLVING THE ortho-HYDROXYL GROUP

Korshunov, S. P.,Korzhova, N. V.,Kazantseva, V. M.,Krasnov, V. L.,Utekhina, N. V.,Bodrikov, I. V.

, p. 1658 - 1663 (2007/10/02)

Amines react with 3-aryl-1--2-propyn-1-ones in three directions, i.e., with addition of the reagent at the triple bond (and the formation of the β-aminovinyl ketone) and intramolecular cyclization leading to the formation of six-membered (flavones) or five-membered (aurones) heterocycles.The development of these reaction paths is controlled by the nature of the amines.Probable reaction paths are proposed.

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