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4-Penten-2-one, 3-methyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135987-22-3

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135987-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135987-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135987-22:
(8*1)+(7*3)+(6*5)+(5*9)+(4*8)+(3*7)+(2*2)+(1*2)=163
163 % 10 = 3
So 135987-22-3 is a valid CAS Registry Number.

135987-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-phenylpent-4-en-2-one

1.2 Other means of identification

Product number -
Other names 3-methyl-1-phenyl-4-penten-2-one

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:135987-22-3 SDS

135987-22-3Downstream Products

135987-22-3Relevant academic research and scientific papers

Indium in organic synthesis: Convenient synthesis of β,γ-unsaturated ketones

Yadav,Srinivas, Dale,Reddy, Gondi Sudershan,Bindu, Konuru Hima

, p. 8745 - 8748 (1997)

A mild and efficient method for the preparation of β,γ unsaturated ketones by a simple reaction on acid chloride with allyl, crotyl, prenyl bromide and indium in DMF is described.

Synthesis of allyl ketone via Lewis acid promoted Barbier-type reaction

Lee,Lin

, p. 8803 - 8806 (2007/10/03)

A series of allyl ketones were synthesized from the mixture of zinc, nitrile and allyl bromide in the presence of AlCl3 via Barbier-type reaction condition. When crotyl bromide was used for the allylation, only the γ-adduct was produced via the

Carbon-carbon bond forming reactions of η3-allyl iron tricarbonyl anions with carbon electrophiles

Chang, Seok,Yoon, Jaeyon,Brookbart, Maurice

, p. 1869 - 1879 (2007/10/02)

Reaction of the η3-allyl iron tricarbonyl anion, 1, with alkyl halides (RX, R = -CH3, -CH2Ph, -(CH2)3CH3, -CH(CH3)2,-CH2CH=CH2) followed by treat

A Practical Synthesis of Rosefuran. Furans from Acetylenes and Allyl Alcohols

Trost, Barry M.,Flygare, John A.

, p. 1078 - 1082 (2007/10/02)

A new atom-economical synthetic strategy for the synthesis of furans emerges from β,γ-unsaturated ketones which are readily available from acetylenes and allyl alcohols by simple additions in the presence of a ruthenium catalyst.Dihydroxylation using cata

Allylation of Aldehydes by Allyl- and Crotyltributyltin in the Presence zof Catalytic Amounts of Bu2SnCl2 Complex

Yano, Katsunori,Baba, Akio,Matsuda, Haruo

, p. 66 - 70 (2007/10/02)

In nearly neutral media, the reaction of allylic tributyltin with aldehydes is effectively catalyzed by Bu2SnCl2 complexes.The addition of coordinative reagents and benzoyl chloride as a quencher is required of the catalytic allylation, furnishing homoall

Allylation of Acid Chlorides by Allyltributyltin in the Presence of Catalytic Amounts of Dibutyltin Dichloride

Yano, Katsunori,Baba, Akio,Matsuda, Haruo

, p. 1181 - 1184 (2007/10/02)

Redistribution of allyltributyltin and dibutyltin dichloride into allyldibutyltin chloride and tributyltin chloride is enhanced by coordinative compounds such as phosphine oxide and ammonium chloride.This redistribution is applied to the reaction of allyl

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