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(1E,2Z)-1,3-diphenylbut-2-en-1-one oxime is a ketoxime chemical compound with the molecular formula C16H15NO. It features a ketone and an oxime functional group, which contribute to its versatile reactivity and structural properties.

5455-12-9

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5455-12-9 Usage

Uses

Used in Organic Synthesis:
(1E,2Z)-1,3-diphenylbut-2-en-1-one oxime is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, playing a crucial role in the development of various organic compounds.
Used in Chemical Reactions:
(1E,2Z)-1,3-diphenylbut-2-en-1-one oxime serves as a reagent in a range of chemical reactions, particularly in the synthesis of heterocyclic compounds, which are important in the creation of complex organic molecules.
Used in Materials Science:
(1E,2Z)-1,3-diphenylbut-2-en-1-one oxime has potential applications in the field of materials science, where its unique properties can be utilized to develop new materials with specific characteristics.
Used in the Synthesis of Complex Organic Molecules:
As a building block, (1E,2Z)-1,3-diphenylbut-2-en-1-one oxime contributes to the construction of complex organic molecules, which are essential in various chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5455-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5455-12:
(6*5)+(5*4)+(4*5)+(3*5)+(2*1)+(1*2)=89
89 % 10 = 9
So 5455-12-9 is a valid CAS Registry Number.

5455-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (NZ)-N-[(Z)-1,3-diphenylbut-2-enylidene]hydroxylamine

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:5455-12-9 SDS

5455-12-9Relevant academic research and scientific papers

Access to Cyclic β-Amino Acids by Amine-Catalyzed Enantioselective Addition of the γ-Carbon Atoms of α,β-Unsaturated Imines to Enals

Luo, Guoyong,Huang, Zhijian,Zhuo, Shitian,Mou, Chengli,Wu, Jian,Jin, Zhichao,Chi, Yonggui Robin

, p. 17189 - 17193 (2019/11/13)

Disclosed herein is a new catalytic approach for an efficient access to cyclic β-amino acids widely found in bioactive small molecules and peptidic foldamers. Our method involves addition of the remote γ-carbon atoms of α,β-unsaturated imines to enals by iminium organic catalysis. This highly chemo- and stereo-selective reaction affords cyclic β-amino aldehydes that can be converted to amino acids bearing quaternary stereocenters with exceptional optical purities. Our study demonstrates the unique power of organic catalytic remote carbon reactions in rapid synthesis of functional molecules.

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