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54074-17-8

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54074-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54074-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,7 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54074-17:
(7*5)+(6*4)+(5*0)+(4*7)+(3*4)+(2*1)+(1*7)=108
108 % 10 = 8
So 54074-17-8 is a valid CAS Registry Number.

54074-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-phenylphenyl) propanoate

1.2 Other means of identification

Product number -
Other names Propionsaeure-biphenyl-2-ylester

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:54074-17-8 SDS

54074-17-8Downstream Products

54074-17-8Relevant articles and documents

PREPARATION AND PROPERTIES OF POLYMERS ANCHORING BIPHENYL-2-OL.

Ishikawa

, p. 2177 - 2178 (1983)

The monomer, 2-biphenyl acrylate (BPA) was prepared and was polymerized and copolymerized with vinyl acetate (VAc), styrene and N-vinylpyrrolidone. The reactivity ratios of BPA(M//1) with VAc were evaluated as r//1 equals 4. 6 plus 0. 4 and r//2 equals 0. 37 plus 0. 08. The polymers were hydrolyzed in methanol-phosphate buffer solution (pH 6 and 8), and the release rate of biphenyl-2-ol from the polymer was investigated. The biphenyl-2-ol could thus be employed as a fungicide over an extended period.

Enzymatic Esterolysis of Polymers Containing 2-Biphenylyl Ester Bonds in Side Chains

Ishikawa, Tomomichi,Otsuki, Makoto,Iwatsuki, Toshiaki

, p. 3621 - 3624 (2007/10/02)

The preparation and α-chymotrypsin-catalyzed esterolysis of polymeric substrates anchoring fungicidal biphenyl-2-ol are described.In order to obtain information regarding the influence of one type of polymeric backbone and the distance between a cleavable bond and a polymer main chain, poly(2-biphenylyl acrylate), poly(2-biphenylyl methacrylate), and poly(methacryloylamino acid 2-biphenylyl ester) were studied.The esterolysis were evaluated by means of Michaelis constant Km and the catalytic reaction rate constant kcat.Poly(2-biphenylyl methacrylate) was a more suitable substrate than poly(2-biphenylyl acrylate).Poly was the most suitable substrate in a series of polymers containing amino acid side chains with 2-biphenylyl ester terminal groups.The release rate of biphenyl-2-ol could also be controlled by using copolymers with an appropriate comonomer.

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