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4362-37-2

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4362-37-2 Usage

Chemical Structure

A dioxolane ring with a chloromethoxy methyl group attached to it.

Usage

Solvent intermediate in the production of pharmaceuticals and pesticides.

Flammability

Flammable, requires careful handling.

Health Hazards

Can cause irritation to the skin, eyes, and respiratory system upon contact.

Safety Precautions

Use of protective equipment and ensuring proper ventilation in the work area is necessary.

Storage and Disposal

Proper storage and disposal methods are crucial to prevent harm to human health or the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 4362-37-2 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 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4362-37:
(6*4)+(5*3)+(4*6)+(3*2)+(2*3)+(1*7)=82
82 % 10 = 2
So 4362-37-2 is a valid CAS Registry Number.

4362-37-2SDS

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 4-(chloromethoxy-methyl)-[1,3]dioxolane

1.2 Other means of identification

Product number -
Other names 4-(Chlormethoxy-methyl)-[1,3]dioxolan

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:4362-37-2 SDS

4362-37-2Downstream Products

4362-37-2Relevant articles and documents

TRINITROETHYL ETHERS OF SUBSTITUTED ALCOHOLS

Luk'yanov, O.A.,Pokhvisneva, G.V.

, p. 2217 - 2221 (2007/10/02)

The influence of the trinitromethane salt cations and the substituents in the alkyl moiety of chloromethyl ethers of alcohols on the yields of trinitroethyl ethers of the substituted alcohols formed from them was established.On this basis a representative series of previously unavailable trinitroethanol ethers was synthesized.

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