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13208-31-6

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13208-31-6 Usage

Chemical class

Urea derivatives

Usage

Fungicide and herbicide

Purpose

Controlling growth of fungi and weeds in agriculture and horticulture

Physical appearance

White, crystalline solid

Taste

Slightly bitter

Solubility

Sparingly soluble in water

Health and environmental risks

Poses risks to human health and the environment

Safety precautions

Handle and apply with caution according to guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 13208-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13208-31:
(7*1)+(6*3)+(5*2)+(4*0)+(3*8)+(2*3)+(1*1)=66
66 % 10 = 6
So 13208-31-6 is a valid CAS Registry Number.

13208-31-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(3-chlorophenyl)urea

1.2 Other means of identification

Product number -
Other names Bis-(3-chlor-phenyl)-formamidin

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:13208-31-6 SDS

13208-31-6Relevant articles and documents

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Price,Leonard,Reitsema

, p. 1256,1258 (1946)

-

Investigation of active sites using solid state 27Al and 31P MAS NMR in ceramic amorphous aluminophosphate materials prepared from different potassium salts of phosphate for the synthesis of diphenyl urea derivatives

Harish,Kathyayini,Baby, Bindhu,Nagaraju

, (2021/04/19)

Ceramic amorphous aluminophosphate (CAmAlP) catalysts were prepared by precipitation method using different phosphate salts of potassium such as KH2PO4, K4P2O7 and K2HPO4 as well as H3PO4. The prepared materials were characterized by PXRD, FT-IR, XPS, SEM, BET Surface area, NH3-TPD, 27Al NMR and 31P NMR analytical methods. The catalytic activity of the materials was checked in the synthesis of diphenyl urea (DPU) from aniline and diethyl carbonate, under refluxing conditions. Further, the general application of the catalysts was tested using various substituted anilines. The recyclability of the catalysts was also studied. Uncertainties in percentage yields were calculated to check the reproducible surface properties. The P-XRD, BET Surface area and NH3-TPD results indicated that the materials were amorphous with mesoporous texture, surface areas and acidities in the range 200–260 m2/g and 0.4–0.7 mmol/g respectively. 27Al NMR studies revealed that Al is present in three different coordination states such as tetrahedral, pentagonal and octahedral. The relative percentages of these Al sites depends on the type of the potassium precursor phosphate salt used. Both tetrahedral and pentagonal Al sites in conjunction with each other represented catalytically active sites. An increase in the pentagonal sites contributed to additional increments to the catalytic activity of CAmAlP. The catalyst prepared from KH2PO4 was found to be the best and demonstrated 96% DPU yield.

N,N'-disubstituted urea compound and synthesis method thereof

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Paragraph 0067-0070, (2019/04/10)

The invention discloses an N,N'-disubstituted urea compound and a preparation method thereof. N-alkyl acyloxy amide is taken as a raw material and a dichloro(p-cymene)ruthenium(II) dimer complex is taken as a catalyst for carrying out a reaction in an organic solvent under the presence of silver acetate, and the N,N'-disubstituted urea compound is prepared. Compared with the prior art, the methodhas the following advantages that only an amide derivative is taken as a raw material, reaction conditions are mild, the application range of substrates is wide, operation is simple and convenient, the catalyst is low in price, and selectivity of the product is high.

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