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18328-11-5

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18328-11-5 Usage

Description

4-PHENYLBUTANAL, with the CAS number 18328-11-5, is an organic compound that serves as a valuable intermediate in the synthesis of various pharmaceuticals and chemicals. It is characterized by its aldehyde functional group and a phenyl group attached to a butyl chain, which contributes to its reactivity and potential applications in different industries.

Uses

Used in Pharmaceutical Industry:
4-PHENYLBUTANAL is used as a reactant for the synthesis of latanoprost, a medication specifically designed to treat increased pressure inside the eye. This application takes advantage of its reactivity in organocatalyzed [3+2]-cycloaddition reactions, which are crucial for the production of latanoprost.

Synthesis Reference(s)

Chemistry Letters, 21, p. 423, 1992Journal of the American Chemical Society, 108, p. 1325, 1986 DOI: 10.1021/ja00266a049Tetrahedron Letters, 34, p. 6505, 1993 DOI: 10.1016/0040-4039(93)88090-6

Check Digit Verification of cas no

The CAS Registry Mumber 18328-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,2 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18328-11:
(7*1)+(6*8)+(5*3)+(4*2)+(3*8)+(2*1)+(1*1)=105
105 % 10 = 5
So 18328-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O/c11-9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7,9H,4-5,8H2

18328-11-5SDS

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 4-PHENYLBUTANAL

1.2 Other means of identification

Product number -
Other names phenylpropylketone

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:18328-11-5 SDS

18328-11-5Relevant articles and documents

An Improved Preparation of Tris(ethylenedioxyboryl)methane, a Reagent for the Homologation of Aldehydes and Ketones

Schummer, Dietmar,Hoefle, Gerhard

, p. 11219 - 11222 (1995)

The preparation of tris(ethylenedioxyboryl)methane (2), the reagent for the only known homologation of aldehydes and ketones under non-acidic conditions, was improved by avoiding the difficult isolation of the intermediate tris(dimethoxyboryl)methane (1) and by direct crystallization of 2.

-

Kumler et al.

, p. 1463,1466 (1950)

-

Intramolecular Aromatic Cyclizations of Alkenyliodonium Tetrafluoroborates

Ochiai, Masahito,Takaoka, Yoshikazu,Sumi, Kenzo,Nagao, Yoshimitsu

, p. 1382 - 1384 (1986)

1,2-Dihydronaphthalene and 2H-chromene derivatives have been synthesized by thermal intramolecular cyclizations of alkenyliodonium tetrafluoroborates under mild reaction conditions.

Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes

Huang, Jiaxin,Li, Jie,Yang, Wen,Zhang, Kezhuo,Zhao, Pei,Zhao, Wanxiang

supporting information, p. 302 - 305 (2022/01/03)

The Co-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes were realized by a ligand-controlled strategy. The remote hydroboration with dcype provided borylethers, while xantphos favored the formation of silyl enol ethers.

Straightforward Synthesis of Fluorinated Enals via Photocatalytic α-Perfluoroalkenylation of Aldehydes

Wulkesch, Christian,Czekelius, Constantin

, p. 7425 - 7438 (2021/06/21)

(Per)fluorinated substances represent an important compound class with regard to drug design and material chemistry. We found a mild, operationally simple, and inexpensive photocatalytic perfluoroalkenylation reaction giving tetrasubstituted, highly electron-deficient enals straight from aldehydes. This one-step reaction tolerates various functional groups and can be applied to a wide range of substrates giving the products in yields of 52-84%.

Pharmacophore-Based Design of Phenyl-[hydroxycyclohexyl] Cycloalkyl-Carboxamide Mitofusin Activators with Improved Neuronal Activity

Bernstein, Peter R.,Dang, Xiawei,Devanathan, Sriram,Dorn, Gerald W.,Franco, Antonietta,Fu, Lijun,Walters, Daniel,Williams, Sidney B.

, p. 12506 - 12524 (2021/09/11)

Mitochondrial fragmentation from defective fusion or unopposed fission contributes to many neurodegenerative diseases. Small molecule mitofusin activators reverse mitochondrial fragmentation in vitro, promising a novel therapeutic approach. The first-in-c

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