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1-phenyl-1,3-dipropan-2-ylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87931-27-9

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87931-27-9 Usage

Compound class

Aromatic monosubstituted ureas

Uses

Production of urethane and other urea compounds, various industrial applications

Physical appearance

White crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Chemical structure

Contains a phenyl group and two propyl groups attached to a urea group

Potential applications

Pharmaceutical, agricultural, and materials science industries

Check Digit Verification of cas no

The CAS Registry Mumber 87931-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,3 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87931-27:
(7*8)+(6*7)+(5*9)+(4*3)+(3*1)+(2*2)+(1*7)=169
169 % 10 = 9
So 87931-27-9 is a valid CAS Registry Number.

87931-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-1,3-di(propan-2-yl)urea

1.2 Other means of identification

Product number -
Other names 1-phenyl-1,3-dipropan-2-yl-urea

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:87931-27-9 SDS

87931-27-9Downstream Products

87931-27-9Relevant academic research and scientific papers

Degradation of O-Arylisoureas in Alkali: A Low-temperature Chapman-type Rearrangement

Suttle, Nicola A.,Williams, Andrew

, p. 1369 - 1372 (2007/10/02)

NN'-Di-isopropyl-O-arylisoureas are demonstrated to rearrange intramolecularly to the corresponding NN'-di-isopropyl-N'-arylurea in alkaline solution.The large negative Broensted-type βL value (-2.3) for the reaction measured against the pK of the corresponding phenol and a modest entropy of activation are consistent with a 1,3-aryl migration.The high efficiency of the migration compared with that of the Chapman rearrangement of O-aryl imidoethers is attributed to the greater internal nucleophilicity of the imino nitrogen, which in the present case bears a negative charge.

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