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1889-01-6

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1889-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1889-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1889-01:
(6*1)+(5*8)+(4*8)+(3*9)+(2*0)+(1*1)=106
106 % 10 = 6
So 1889-01-6 is a valid CAS Registry Number.

1889-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(2-chloro-2-oxoethoxy)phenoxy]acetyl chloride

1.2 Other means of identification

Product number -
Other names p-phenylenedioxydi-acetyl chloride

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:1889-01-6 SDS

1889-01-6Relevant articles and documents

Phase transfer catalyzed synthesis of diaryl 1,4-phenylene dioxydiacetate

Wei, Taibao,Chen, Jichou,Wang, Xicun,Zhang, Youming,Wang, Lailai

, p. 1447 - 1454 (1996)

The title compounds 3a-3o were prepared with high yield via the reaction of 1,4-phenylenedioxydiacetyl chloride with various substituted phenols under the condition of liquid-liquid phase transfer catalysis, using polyethylene glycol - 400 as the catalyst.

Functionalized biodegradable triclosan monomers and oligomers for controlled release

-

Page/Page column 58, (2011/11/13)

This invention relates to the discovery of functionalized triclosan monomers and oligomers that, when incorporated into a substrate of, or applied as part of a coating to, medical devices and/or consumer products may extend the duration of antimicrobial properties to the medical devices and/or consumer products.

Dihydroxy aromatic compounds and methods for preparation

-

Page/Page column 15, (2010/11/25)

A dihydroxy aromatic compound having a Formula (I), wherein R1 is a C6–C60 aromatic divalent functionality, R2 at each occurrence, can be the same or different and is independently at each occurrence selected from the group consisting of a cyano functionality, a nitro functionality, a halogen, an aliphatic functionality having 1 to 10 carbons, a cycloaliphatic functionality having 3 to 10 carbons and an aromatic functionality having 6 to 10 carbons, and “n” is an integer having a value of 0 to 4.

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