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24420-88-0

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24420-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24420-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,2 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24420-88:
(7*2)+(6*4)+(5*4)+(4*2)+(3*0)+(2*8)+(1*8)=90
90 % 10 = 0
So 24420-88-0 is a valid CAS Registry Number.

24420-88-0SDS

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 ethyl 3-hydroxy-3-methylhexanoate

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-3-methyl-hexansaeure-aethylester

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:24420-88-0 SDS

24420-88-0Relevant articles and documents

Unique Molecular Discrimination in Europium Complex-Catalyzed Reactions of Saturated and α,β-Unsaturated Ketones with Ketene Silyl Acetals

Hanyuda, Kiyoshi,Hirai, Kei-Ichi,Nakai, Takeshi

, p. 31 - 32 (1997)

The unique molecular discriminations are observed in the Eu(III)-catalyzed reactions of saturated ketones, α,β-enones, and α,β-ynones with ketene silyl acetals and discussed in terms of the discriminating ability of the Eu-catalyst at the complexation sta

Metal Exchange between an Electrogenerated Organonickel Species and Zinc Halide: Application to an Electrochemical, Nickel-Catalyzed Reformatsky Reaction

Conan, Annie,Sibille, Soline,Perichon, Jacques

, p. 2018 - 2024 (2007/10/02)

The mechanism of the electroreductive coupling of α-chloro esters or α-chloro nitriles with carbonyl compounds by the means of a sacrificial zinc anode and a nickel catalyst was elucidated by electroanalytical techniques.The mechanism involved reduction of a Ni(II) complex to a Ni(0) complex, oxidative addition of the α-chloro ester to the Ni(0) complex, and a Zn(II)/Ni(II) exchange, leading to an organozinc Reformatsky reagent.The electrosynthesis of various β-hydroxy esters, β-hydroxy nitriles, and 2,3-epoxy esters was successfully achieved under extremely mild conditions.

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