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64479-84-1

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64479-84-1 Usage

General Description

(3-HYDROXYPHENYL)ACETONE, also known as 3-Hydroxyacetophenone, is a chemical compound with the molecular formula C8H8O2. It is a white crystalline solid with a sweet, floral odor. 3-Hydroxyacetophenone is commonly used in the production of perfumes and fragrances due to its pleasant scent. It is also used as a flavoring agent in the food industry. Additionally, this chemical compound has anti-inflammatory properties and is being studied for its potential medicinal uses. It is important to handle (3-HYDROXYPHENYL)ACETONE with care and follow safety protocols when working with it, as it may cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 64479-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64479-84:
(7*6)+(6*4)+(5*4)+(4*7)+(3*9)+(2*8)+(1*4)=161
161 % 10 = 1
So 64479-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c1-7(10)5-8-3-2-4-9(11)6-8/h2-4,6,11H,5H2,1H3

64479-84-1SDS

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 1-(3-hydroxyphenyl)propan-2-one

1.2 Other means of identification

Product number -
Other names 2-Propanone,1-(3-hydroxyphenyl)

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:64479-84-1 SDS

64479-84-1Downstream Products

64479-84-1Relevant articles and documents

Transaminase-Mediated Amine Borrowing via Shuttle Biocatalysis

O'Reilly, Elaine,O'Sullivan, Rachel,Ryan, James,Taday, Freya

supporting information, (2022/01/04)

Shuttle catalysis has emerged as a useful methodology for the reversible transfer of small functional groups, such as CO and HCN, and goes far beyond transfer hydrogenation chemistry. While a biocatalytic hydrogen-borrowing methodology is well established, the biocatalytic borrowing of alternative functional groups has not yet been realized. Herein, we present a new concept of amine borrowing via biocatalytic shuttle catalysis, which has no counterpart in chemo-shuttle catalysis and allows efficient intermolecular amine shuttling to generate reactive intermediates in situ. By coupling this dynamic exchange with an irreversible downstream step to displace the reaction equilibrium in the forward direction, high conversion to target products can be achieved. We showcase the potential of this amine-borrowing methodology using a biocatalytic equivalent of both the Knorr-pyrrole synthesis and Pictet-Spengler reaction.

Crystal form of L-lysinate of benzopiperidine derivative and preparation method thereof

-

Paragraph 0076; 0080-0082, (2020/07/15)

The invention provides a crystal form of a L-lysinate of a benzopiperidine derivative and a preparation method of the crystal form. Specifically, the invention provides a crystal form II of L-lysinateof (E)-3-(4-((1R, 3R)-2-(4-cyclopropyl phenyl)-6-(1-ethyl-1H-pyrazol-4-yl)-3-methyl-1, 2, 3, 4-tetrahydroisoquinoline-1-yl) phenyl) acrylate and a preparation method of the crystal form II. The crystal form II of the compound shown in the formula (I) has good stability and can be better applied to clinical treatment.

Compositions and methods for determining the presence of amphetamines in a sample suspected of containing amphetamine and/or methamphetamine

-

, (2008/06/13)

The instant invention is directed toward an immunoassay which can determine the presence of amphetamines in a sample suspected of containing amphetamine and/or methamphetamine by employing at least two conjugates, each comprised of a functionally similar label bound to an amphetamine analog and a methamphetamine analog respectively and an antibody to amphetamine and an antibody to methamphetamine wherein at least one of the antibodies is a monoclonal antibody.

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