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4360-58-1

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4360-58-1 Usage

General Description

2,4,4,5,5-pentamethyl-1,3-dioxolane is a chemical compound with the molecular formula C10H20O2. It is a colorless liquid with a slightly sweet odor, and it is primarily used as a solvent and in various industrial applications. This chemical is also commonly known as PMDO and is known for its ability to dissolve a wide range of organic compounds. It is considered to be relatively stable and non-reactive, making it a versatile and valuable solvent in various industrial processes. Additionally, it is known for its low toxicity and is considered to be generally safe for use when handling under appropriate safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 4360-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4360-58:
(6*4)+(5*3)+(4*6)+(3*0)+(2*5)+(1*8)=81
81 % 10 = 1
So 4360-58-1 is a valid CAS Registry Number.

4360-58-1SDS

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 2,4,4,5,5-Pentamethyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names pinacol methylboronate

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:4360-58-1 SDS

4360-58-1Relevant articles and documents

Catalytic migratory oxidative coupling of nitrones

Hashizume, Shogo,Oisaki, Kounosuke,Kanai, Motomu

supporting information; experimental part, p. 4288 - 4291 (2011/10/09)

A Cu(I)-catalyzed migratory oxidative coupling between nitrones and heterocycles or a methylamine is described. Selective C-C bond-formation proceeds through cleavage of two C(sp3)-H bonds concomitant with C=N double bond-migration. The reaction provides an alternating nitrone moiety, allowing for further synthetically useful transformations. Radical clock studies suggest that the nucleophilic addition of nitrones to an oxidatively generated carbocation is a key step.

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