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617-07-2

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617-07-2 Usage

Description

SYM-DI-O-TOLYLUREA, also known as di-o-tolylurea, is a white crystalline solid that is insoluble in water and most organic solvents. It is a chemical compound used as a raw material in the production of various industrial products.

Uses

Used in Chemical Industry:
SYM-DI-O-TOLYLUREA is used as an intermediate in the production of dyes, pigments, and pharmaceuticals. It plays a crucial role in the synthesis of these compounds, contributing to their color and properties.
Used in Polymer Manufacturing:
SYM-DI-O-TOLYLUREA is used as a stabilizer in the manufacturing of polymers. It helps to improve the stability and durability of the polymers, enhancing their performance in various applications.
Used in Rubber Production:
SYM-DI-O-TOLYLUREA is used as a crosslinking agent in the production of rubber products. It aids in the formation of a network structure in rubber, improving its strength and elasticity.
Used in Synthesis of Other Organic Compounds:
SYM-DI-O-TOLYLUREA is used in the synthesis of other organic compounds, contributing to the development of new materials and products.
Used in Agricultural Applications:
SYM-DI-O-TOLYLUREA is used as a pesticide in agricultural applications. It helps to protect crops from pests and diseases, ensuring a healthy and productive harvest.

Check Digit Verification of cas no

The CAS Registry Mumber 617-07-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 617-07:
(5*6)+(4*1)+(3*7)+(2*0)+(1*7)=62
62 % 10 = 2
So 617-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N2O/c1-11-7-3-5-9-13(11)16-15(18)17-14-10-6-4-8-12(14)2/h3-10H,1-2H3,(H2,16,17,18)

617-07-2SDS

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(2-methylphenyl)urea

1.2 Other means of identification

Product number -
Other names Carbanilide,2,2'-dimethyl

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:617-07-2 SDS

617-07-2Relevant articles and documents

Palladium-Catalyzed Aerobic Oxidative Carbonylation of Amines Enables the Synthesis of Unsymmetrical N,N′-Disubstituted Ureas

Zeng, Honglan,Du, Hongyan,Gong, Xu,Zhang, Jie,Han, Wei

, p. 1223 - 1226 (2021/06/02)

A ligand-free palladium-catalyzed aerobic oxidative carbonylation of amines for the synthesis of ureas, particular unsymmetrically N,N′-disubstituted ureas, which cannot be accessed by any other palladium-catalyzed oxidative carbonylation of amines to date, is presented. An array of symmetrical and unsymmetrical ureas were straightforwardly synthesized by using inexpensive, readily available, stable, and safe amines with good to excellent yields under a pressure of 1 atm. This novel method employs oxygen as the sole oxidant and offers an attractive alternative to transition-metal-based oxidant systems.

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.

2,2′,2″-(2,4,6-Trioxo-1,3,5-triazinane-1,3,5-triyl)triacetic Acid Derivatives. New Aspects of Reactivity

Kavina, M. A.,Sizov, V. V.

, p. 1046 - 1053 (2020/08/28)

Abstract: Reaction of 2,2′,2″-(2,4,6-trioxo-1,3,5-triazinane-1,3,5-triyl)triacetic acid derivatives with nucleophiles in aqueous medium involved opening of the triazinane ring with elimination of carbonyl group, followed by recyclization to 1-carbamoylhydantoins.

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