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Cyanic acid, 3-chlorophenyl ester, also known as 3-chlorophenyl cyanate, is an organic compound with the chemical formula C8H6ClNO. It is a derivative of cyanic acid, where a 3-chlorophenyl group replaces the hydrogen atom in the hydroxyl group. This colorless to pale yellow liquid is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is characterized by its reactivity, particularly in nucleophilic substitution reactions, and is known for its potential to form isocyanates, which are important in the production of polyurethanes and other polymers. Due to its reactivity and potential health hazards, it is important to handle 3-chlorophenyl cyanate with care, following proper safety protocols.

1124-37-4

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1124-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1124-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1124-37:
(6*1)+(5*1)+(4*2)+(3*4)+(2*3)+(1*7)=44
44 % 10 = 4
So 1124-37-4 is a valid CAS Registry Number.

1124-37-4SDS

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 (3-chlorophenyl) cyanate

1.2 Other means of identification

Product number -
Other names m-Chloro-phenylcyanat

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:1124-37-4 SDS

1124-37-4Relevant academic research and scientific papers

Synthesis and structure of substituted 5-phenoxy-1,2,4-dithiazole-3-ones

Ponomarov, Oleksandr,Padelkova, Zdenka,Hanusek, Jiri

, p. 1225 - 1228 (2011)

Seven new substituted 5-phenoxy-1,2,4-dithiazole-3-ones were prepared in modest yield (53-76%) from corresponding O-phenyl thiocarbamates and chlorocarbonylsulfenyl chloride in dry ether at-10 °C. All of the compounds were characterized by NMR and elemental analysis and some of them by X-ray diffraction. Preliminary kinetic measurements showed that the parent 5-phenoxy-1,2,4-dithiazole-3-one is a very efficient sulfurizing agent toward triphenyl phosphite. Copyright

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