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4-(chloromethyl)-2-(4-methoxyphenyl)-1,3-dioxolane is a chemical compound with the molecular formula C10H11ClO3. It is a colorless liquid with a molecular weight of 214.65 g/mol. 4-(chloromethyl)-2-(4-methoxyphenyl)-1,3-dioxolane is characterized by the presence of a chloromethyl group (-CH2Cl) at the 4-position, a 4-methoxyphenyl group (-OCH3) attached to the 2-position, and a 1,3-dioxolane ring structure. The 1,3-dioxolane ring consists of two oxygen atoms and three carbon atoms, forming a five-membered cyclic ether. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antibiotics and antifungal agents. Due to its reactivity, it is essential to handle 4-(chloromethyl)-2-(4-methoxyphenyl)-1,3-dioxolane with care, following proper safety protocols and guidelines.

4469-48-1

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4469-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4469-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4469-48:
(6*4)+(5*4)+(4*6)+(3*9)+(2*4)+(1*8)=111
111 % 10 = 1
So 4469-48-1 is a valid CAS Registry Number.

4469-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(chloromethyl)-2-(4-methoxyphenyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names anisyl-2 chloromethyl-4 dioxolanne-1,3

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:4469-48-1 SDS

4469-48-1Relevant academic research and scientific papers

FORMATION DE DIOXOLANNES A PARTIR DE L'EPICHLORHYDRINE DU GLYCEROL. HYDROLYSE AISEE DE DIOXOLANNES PAR LE TOSYLATE DE PYRIDINIUM

Thuy, Vu Moc,Petit, Huguette,Maitte, Pierre

, p. 759 - 762 (2007/10/02)

We described a versatile synthesis of dioxolanne from 1-chlor 2,3-epoxypropane epichlorhydrine and different carbonyl compounds in presence of activated montmorillonite which is easily eliminated after the reaction.The hydrolysis was performed in mild conditions with pyridinium p-toluene sulfonate.

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