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O-isopropyl-N,N'-dicyclohexyl-isourea is a complex organic compound with the chemical formula C18H32N2O. It is a white crystalline solid that is soluble in organic solvents. O-isopropyl-N,N'-dicyclohexyl-isourea is characterized by its unique structure, featuring an isourea group (a urea derivative with one of the oxygen atoms replaced by a carbonyl group), an isopropyl group (a propyl group with one of the hydrogen atoms replaced by a methyl group), and two cyclohexyl groups (cyclic structures with six carbon atoms). O-isopropyl-N,N'-dicyclohexyl-isourea is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Its specific applications may vary, but its role in these industries is significant due to its ability to form stable and effective compounds.

6804-20-2

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6804-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6804-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6804-20:
(6*6)+(5*8)+(4*0)+(3*4)+(2*2)+(1*0)=92
92 % 10 = 2
So 6804-20-2 is a valid CAS Registry Number.

6804-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dicyclohexyl-O-(1'-methylethyl)isourea

1.2 Other means of identification

Product number -
Other names N,N'-Dicyclohexyl-O-isopropyl-isoharnstoff

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:6804-20-2 SDS

6804-20-2Relevant academic research and scientific papers

One pot conversion of alcohols to disulfides mediated by benzyltriethylammonium tetrathiomolybdate

Sinha, Surajit,Ilankumaran,Chandrasekaran

, p. 14769 - 14776 (2007/10/03)

A one pot conversion of alcohols to disulfides in good yields via the activation of a hydroxyl group with DCC or P(NMe2)3 / CCl4 followed by treatment with benzyltriethylammonium tetrathiomolybdate is reported.

Novel steroids

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, (2008/06/13)

Novel steroids of the formula STR1 wherein R is selected from the group consisting of R1 and R2, R1 is selected from the group consisting of alkyl of 1 to 8 carbon atoms and alkenyl and alkynyl of 2 to 8 carbon atoms R2 is --(CH2)n --R3, n is an integer from 1 to 8 and R3 is selected from the group consisting of free or protected --OH, free or protected --NH2, monoalkyl and dialkylamino with 1 to 6 carbon atoms, a free, esterified or salified --COOH and halogen X and Y together form STR2 or X is OH and Y is --CH2 --CH2 --COOM, M is selected from the group consisting of hydrogen, an alkali metal and --NH4, Ra is selected from the group consisting of hydrogen and methyl, the dotted line in the I(2)-position indicates the optional presence of a double bond and the wavy line indicates that R may be in the α- or β-position, with the proviso that R is not R1 or R2 when n is 1 and R3 is halogen, when the 1(2) bond is a simple bond and when Ra is --CH3, R3 is not a free carboxyl when Y is --CH2 --CH2 --COOM in which M is an alkali metal or --NH4 and R3 is not a salified carboxyl when Y is --CH2 --CH2 --COOH having aldosterone antagonistic properties and increases aqueous sodium diuresis while conserving organic potassium without secondary hormonal effects and their preparation.

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