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15866-63-4

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15866-63-4 Usage

Classification

Nitro compound A category of compounds that includes a nitro group (-NO2) bonded to an aromatic ring.

Structure

Nitro group attached to a benzene ring, with a conjugated phenylbutadiene moiety A description of the compound's molecular structure, including the arrangement of functional groups.

Application

Organic synthesis The compound is used as a building block in the production of other chemical compounds.

Usage

Chemical intermediate The compound serves as an intermediate step in the manufacturing of various products, such as dyes, pigments, and pharmaceuticals.

Potential

Medicinal chemistry and research The molecular structure of the compound suggests its possible use in the development of new drugs and scientific studies.

Check Digit Verification of cas no

The CAS Registry Mumber 15866-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15866-63:
(7*1)+(6*5)+(5*8)+(4*6)+(3*6)+(2*6)+(1*3)=134
134 % 10 = 4
So 15866-63-4 is a valid CAS Registry Number.

15866-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-3-[(1Z,3E)-4-phenylbuta-1,3-dienyl]benzene

1.2 Other means of identification

Product number -
Other names 1-m-Nitrophenyl-4-phenyl-1,3-butadien

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:15866-63-4 SDS

15866-63-4Relevant articles and documents

Site-Selective Nitrene Transfer to Conjugated Olefins Directed by Oxazoline Peptide Ligands

Storch, Golo,van den Heuvel, Naudin,Miller, Scott J.

, p. 289 - 294 (2019/08/30)

Site-selective nitrene transfer to di- and polyene substrates has been achieved using designed peptide-embedded bioxazoline ligands capable of binding copper. In model 1,3-diene substrates, the olefinic position proximal to a directing group was selectively functionalized. Additional studies indicate that this selectivity stems from non-covalent substrate-catalyst interactions. The peptide-mediated nitrene transfer was also applied to polyene natural product retinol and selective proximal functionalization allowed access to a cis-pyrroline modified retinoid. (Figure presented.).

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