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157953-22-5

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157953-22-5 Usage

General Description

Ethanone, 1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]- is a complex chemical compound with a molecular structure that includes a ketone group and a combination of hydroxy, methyl, butynyl, and phenyl groups. Ethanone, 1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]- is a derivative of the natural compound resveratrol and belongs to a group of chemicals known as stilbenoids. It is known for its potential antioxidant, anti-inflammatory, and anti-cancer properties. Research suggests that this compound may have potential therapeutic effects against various diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases. However, further studies are needed to fully understand its biological activities and potential medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 157953-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,9,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157953-22:
(8*1)+(7*5)+(6*7)+(5*9)+(4*5)+(3*3)+(2*2)+(1*2)=165
165 % 10 = 5
So 157953-22-5 is a valid CAS Registry Number.

157953-22-5SDS

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 1-[4-Benzyloxy-3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-ethanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:157953-22-5 SDS

157953-22-5Relevant articles and documents

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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