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111728-87-1

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111728-87-1 Usage

Type

Organic compound

Structure

Consists of a benzene ring with a hydroxyl group and a 4-(2-chloroethoxy) side chain attached

Uses

Solvent, intermediate, reagent in organic synthesis

Reactivity

2-chloroethoxy group adds reactivity and functionality to molecule

Applications

Production of pharmaceuticals, agrochemicals, industrial products

Safety

Must be handled with caution as it may be hazardous if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 111728-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,7,2 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111728-87:
(8*1)+(7*1)+(6*1)+(5*7)+(4*2)+(3*8)+(2*8)+(1*7)=111
111 % 10 = 1
So 111728-87-1 is a valid CAS Registry Number.

111728-87-1SDS

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 [4-(2-Chloroethoxy)phenyl]methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,4-(2-chloroethoxy)

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:111728-87-1 SDS

111728-87-1Relevant articles and documents

USE OF DISUBSTITUTED BENZENES TO CONTROL INSECTICIDE-RESISTANT PESTS

-

Page/Page column 35; 36; 39; 40, (2018/11/26)

The invention is in the technical field of insect control and relates to the use of a disubstituted benzenes for controlling insecticide-resistant pests such as mosquitoes and cockroaches.

Novel purine nitrile derived inhibitors of the cysteine protease cathepsin K

Altmann, Eva,Cowan-Jacob, Sandra W.,Missbach, Martin

, p. 5833 - 5836 (2007/10/03)

Starting from the high-throughput screening hit 1a, novel cathepsin K inhibitors have been developed based on a purine scaffold. High-resolution X-ray structures of several derivatives have revealed the binding mode of these unique cysteine protease inhib

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