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Ethane-1,2-diyl bis(phenylcarbamate), also known as ethylene bis(phenylcarbamate) or simply phenylcarbamate, is an organic compound with the chemical formula C15H14N2O2. It is a white crystalline solid that is formed by the reaction of ethylene glycol and phenyl isocyanate. ethane-1,2-diyl bis(phenylcarbamate) is primarily used as a precursor in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. It is known for its potential use in the production of herbicides and insecticides due to its carbamate structure, which is a common feature in many pesticides. The compound is also of interest in the field of materials science for its potential applications in the development of new polymers and other advanced materials.

849-98-9

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849-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849-98-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 849-98:
(5*8)+(4*4)+(3*9)+(2*9)+(1*8)=109
109 % 10 = 9
So 849-98-9 is a valid CAS Registry Number.

849-98-9SDS

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 2-(phenylcarbamoyloxy)ethyl N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names Phenyl-<2-phenyl-carbamoyloxy-ethyl>-urethan

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:849-98-9 SDS

849-98-9Downstream Products

849-98-9Relevant academic research and scientific papers

Condensation reactions of benzils with ureas in ethylene glycol

Lee, Chang Kiu,Kim, Sun Hee,Kim, Yong Bun

, p. 1019 - 1024 (2007/10/03)

Reactions of benzils and urea in ethylene glycol at 180° for 1-2 hours gave 2,4,5-triaryloxazoles as major products and bicyclic imidazoimidazole-2,5-diones as minor products. N-Methylurea and W-phenylurea gave the oxazoles under similar conditions. The solvent seemed to assist the formation of oxazole by eliminating the isocyanate components as ethylene glycol biscarbamates.

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