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3-Pentanone, 2-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107798-64-1

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107798-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107798-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,9 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107798-64:
(8*1)+(7*0)+(6*7)+(5*7)+(4*9)+(3*8)+(2*6)+(1*4)=161
161 % 10 = 1
So 107798-64-1 is a valid CAS Registry Number.

107798-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylmethoxypentan-3-one

1.2 Other means of identification

Product number -
Other names 2-benzyloxy-3-pentanone

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:107798-64-1 SDS

107798-64-1Relevant academic research and scientific papers

Optical resolution of acyclic α-hydroxy ketone derivatives by inclusion complexation

Matsumoto, Kazutsugu,Okamoto, Tomomi,Otsuka, Keiko

, p. 2051 - 2056 (2007/10/03)

A new method for the preparation of optically active acyclic α-hydroxy ketone derivatives by thermodynamic resolution using a chiral host compound is described. We examined the resolution of racemic 2-benzyloxy-3-pentanone with chiral host compounds in va

Preparation of Optically Active α-Hydroxy Ketone Derivatives by Enzyme-Mediated Hydrolysis of Enol Esters

Matsumoto, Kazutsugu,Suzuki, Natsuko,Ohta, Hiromichi

, p. 7159 - 7162 (2007/10/02)

A new method of preparation of optically active α-hydroxy ketone derivatives has been developed.Incubation of (Z)-3-propionyloxy-4-benzyloxy-2-pentene (1a) with lipase OF gave optically pure (R)-enol propionate 1a, which in turn was converted without racemization to (R)-ketone 2a by the aid of LiAlH4.

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