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24262-65-5

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24262-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24262-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24262-65:
(7*2)+(6*4)+(5*2)+(4*6)+(3*2)+(2*6)+(1*5)=95
95 % 10 = 5
So 24262-65-5 is a valid CAS Registry Number.

24262-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl 4-acetyloxybenzoate

1.2 Other means of identification

Product number -
Other names phenyl p-acetoxybenzoate

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:24262-65-5 SDS

24262-65-5Relevant articles and documents

Cu(II)-silsesquioxanes as efficient precatalysts for Chan-Evans-Lam coupling

Astakhov, G. S.,Bantreil, X.,Bilyachenko, A. N.,Dorovatovskii, P. V.,Khrustalev, V. N.,Lamaty, F.,Levitsky, M. M.,Shubina, E. S.,Zubavichus, Y. V.

, (2019/11/28)

Two cage copper(II)silsesquioxanes, namely, tricopper complex (PhSiO1.5)8(CuO)3(TMEDA)2*(MeCN)3 Cu-1 and hexacopper complex (MeSiO1,5)12(CuO)6(Py)6*TMEDA Cu

Enzymatic hydrolyses of acetoxy- and phenethylbenzoates by Candida cylindracea lipase

Cipiciani, Antonio,Fringuelli, Francesco,Scappini, Anna Maria

, p. 9869 - 9876 (2007/10/03)

The lipase from Candida cylindracea (CCL) deacctyles rapidly and selective all three regioisomer methyl acctoxybenzoates. In the enzymatic hydrolyses of analogous aryl acctoxybenzoates, the difference of reactivity between the acetoxy and benzoloxy funcionalities is reduced and a aspirin- like prodrugs. The degree of enantioselectivity of the enzymatic hydrolysis of phenethylbenzoates is related to the position of the stereogenic center.

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