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824-90-8

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824-90-8 Usage

Physical state

Colorless liquid
The compound exists in a liquid form and is colorless in appearance.

Odor

Fruity
1-phenyl-1-butene has a pleasant, fruity smell.

Solubility

Soluble in organic solvents
The compound can dissolve in many organic solvents, making it compatible with various chemical processes.

Usage in perfumes and cosmetics

Fragrance ingredient
Due to its fruity odor, 1-phenyl-1-butene is used as a fragrance ingredient in perfumes and cosmetics.

Usage in food products

Flavoring agent
The compound can also be used to add flavor to food products, enhancing their taste and aroma.

Synthesis of other organic compounds

Starting material
1-phenyl-1-butene serves as a starting material in the synthesis of various other organic compounds, such as pharmaceuticals and agrochemicals.

Safety precautions

Flammable, harmful if swallowed or inhaled
It is important to handle 1-phenyl-1-butene with care, as it is flammable and may pose health risks if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 824-90-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 824-90:
(5*8)+(4*2)+(3*4)+(2*9)+(1*0)=78
78 % 10 = 8
So 824-90-8 is a valid CAS Registry Number.

824-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)/(Z)-1-phenylbut-1-en

1.2 Other means of identification

Product number -
Other names β-ethyl styrene

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:824-90-8 SDS

824-90-8Relevant articles and documents

Trifluoroacetic Acid Catalyzed Allylic Phenylation of α-Methylallyl Acetate, α-Methylallyl Trifluoroacetate, and α-Methylallyl Alcohol with Benzene

Fujiwara, Yuzo,Kuromaru, Hiroaki,Taniguchi, Hiroshi

, p. 4309 - 4310 (1984)

-

Quaternary Phosphonium Carboxylates: Structure, Dynamics and Intriguing Olefination Mechanism

Müller-Bunz, Helge,Muldoon, Jimmy,Nikitin, Kirill,Vetter, Anna C.

supporting information, (2022/01/12)

We have earlier shown how the Wittig chemistry can be done using novel Eigenbase phosphonium carboxylate reagents. Here we discuss the phenomenon of ion pairing, their solution tautomerism, solid-state structure, and mechanistic aspects of olefination. The results point to a complex process involving unfamiliar H-bond-driven ion-pair equilibria followed by standard Wittig reaction steps.

Synthesis and catalytic application of new [{IrCl(cod)}2(μ2-diNHC)] and [{Ir(cod)(sulfonated phosphine)}2(μ2-diNHC)] complexes

Czégéni, Csilla Enik?,Horváth, Henrietta,Joó, Ferenc,Kathó, ágnes,Marozsán, Natália,Orosz, Krisztina,Papp, Gábor,Udvardy, Antal

, (2022/01/20)

Four new dinuclear iridium(I) complexes were synthesized from the di(N-heterocyclic carbene) ligand precursors 1,1′-methylene-bis(3-benzyl-imidazolium)dichloride and 1,1′-methylene-bis(3-(2,4,6-trimethylbenzyl)imidazolium)dichloride. The complexes were fu

A Simple Nickel Catalyst Enabling an E-Selective Alkyne Semihydrogenation

Thiel, Niklas O.,Kaewmee, Benyapa,Tran Ngoc, Trung,Teichert, Johannes F.

, p. 1597 - 1603 (2020/02/05)

Stereoselective alkyne semihydrogenations are attractive approaches to alkenes, which are key building blocks for synthesis. With regards to the most atom-economic reducing agent dihydrogen (H2), only few catalysts for the challenging E-selective alkyne semihydrogenation have been disclosed, each with a unique substrate scope profile. Here, we show that a commercially available nickel catalyst facilitates the E-selective alkyne semihydrogenation of a wide variety of substituted internal alkynes. This results in a simple and broadly applicable overall protocol to stereoselectively access E-alkenes employing H2, which could serve as a general method for synthesis.

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