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1489-69-6

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1489-69-6 Usage

Chemical Properties

clear colorless liquid

Description

Cyclopropanecarboxaldehyde can react with Grignard or organolithium reagents to give the expected secondary alcohols. These are susceptible to ring opening in the presence of HBr, providing stereoselective access to homoallylic bromides. It is also used in the synthesis of eta(2)-enonenickel complexes by reacting with [Ni(cod)(2)] (cod = 1,5-cyclooctadiene) and PBu(3) and to prepare a cyclopropylidene tetralone which underwent an enantioselective palladium-catalyzed [3+2] TMM cycloaddition providing a chiral spiro-fused cyclopentene1-2. It is also a reagent in the preparation of N-alkylphenylalaninamides of pyridinylphenyl- and oxobipyridinylamines as human GPR 142 agonists for potential use as anti-diabetic agents and the cytochrome P 450 inhibition3.

Uses

suzuki reaction
InChI:InChI=1/C4H6O/c5-3-4-1-2-4/h3-4H,1-2H2

1489-69-6 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (L14931)  Cyclopropanecarboxaldehyde, 98%    1489-69-6 5g 815.0CNY Detail
Alfa Aesar (L14931)  Cyclopropanecarboxaldehyde, 98%    1489-69-6 1g 293.0CNY Detail

1489-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopropanecarboxaldehyde

1.2 Other means of identification

Product number -
Other names Cyclopropanecarboxaldehyde

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:1489-69-6 SDS

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