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1-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26932-05-8

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26932-05-8 Usage

Preparation

Obtained by reaction of 2-methyl-3-buten-2-ol with 4-hydroxyacetophenone in the presence of boron trifluoride etherate.

Check Digit Verification of cas no

The CAS Registry Mumber 26932-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,3 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26932-05:
(7*2)+(6*6)+(5*9)+(4*3)+(3*2)+(2*0)+(1*5)=118
118 % 10 = 8
So 26932-05-8 is a valid CAS Registry Number.

26932-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxy-3-(3-methylbut-2-enyl)phenyl)ethanone

1.2 Other means of identification

Product number -
Other names 3-[3,3-dimethylallyl]-p-hydroxyacetophenone

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:26932-05-8 SDS

26932-05-8Relevant academic research and scientific papers

First total synthesis of highly anti-inflammatory active licochalcone d through water-accelerated [3,3]-sigmatropic rearrangement

Kim, Si-Jun,Jun, Jong-Gab

, p. 54 - 58 (2013/08/24)

Licochalcones, derived from the dried roots of Glycyrrhiza inflata, have been reported to show various biological activities including antitumor, antiparasitic, antileishmanial, antioxidative, superoxide scavenging, antibacterial, and PTP1B activity. Lico

Design, synthesis, and evaluation of bromo-retrochalcone derivatives as protein tyrosine phosphatase 1B inhibitors

Liu, Zhiguo,Lee, Woojung,Kim, Su-Nam,Yoon, Goo,Cheon, Seung Hoon

supporting information; experimental part, p. 3755 - 3758 (2011/08/06)

A series of bromo-retrochalcones was designed, synthesized and evaluated as PTP1B inhibitors based on licochalcone A and E. Compounds 6, 12, 13, 14, 25, 36, 37, 39, and 41 showed potent inhibitory effects against PTP1B, and compound 37, the most potent am

Regioselectivity in the ene reaction of singlet oxygen with ortho-prenylphenol derivatives

Helesbeux, Jean-Jacques,Duval, Olivier,Guilet, David,Séraphin, Denis,Rondeau, David,Richomme, Pascal

, p. 5091 - 5104 (2007/10/03)

The ene reaction of singlet oxygen with prenylated dihydroxyacetophenones led to the 2-hydroperoxy-3-methylbut-3-enyl derivatives as the major product. This original regioselectivity outlined a new effect, in competition with the previously established la

REGIOSELECTIVE PRENYLATION OF PHENOLS BY PALLADIUM CATALYST: SYNTHESES OF PRENYLPHENOLS AND CHROMANS

Tsukayama, Masao,Kikuchi, Makoto,Kawamura, Yasuhiko

, p. 1487 - 1490 (2007/10/02)

The palladium-catalyzed coupling reaction of iodophenols (1) with 2-methyl-3-butyn-2-ol gave alkynylphenols (2).Catalytic hydrogenation of 2 over Raney nickel and the subsequent dehydration of the resultant alkylphenols (3) gave regioselectively the desired prenylphenols (4).Dehydration of alkylphenols (3f-h) gave chromans (7).

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