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phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 439680-99-6 Structure
  • Basic information

    1. Product Name: phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate
    2. Synonyms: phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate
    3. CAS NO:439680-99-6
    4. Molecular Formula:
    5. Molecular Weight: 450.578
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 439680-99-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate(439680-99-6)
    11. EPA Substance Registry System: phenyl N-[4-({4-[(phenoxycarbonyl)amino]cyclohexyl}methyl)cyclohexyl]carbamate(439680-99-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 439680-99-6(Hazardous Substances Data)

439680-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439680-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,8 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 439680-99:
(8*4)+(7*3)+(6*9)+(5*6)+(4*8)+(3*0)+(2*9)+(1*9)=196
196 % 10 = 6
So 439680-99-6 is a valid CAS Registry Number.

439680-99-6Relevant articles and documents

METHOD FOR PRODUCING CARBAMATE AND METHOD FOR PRODUCING ISOCYANATE

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Paragraph 0367-0368; 0379; 0399-0401; 0403, (2021/06/22)

The present invention provides a method for producing a carbamate that includes a step (1) and a step (2) described below: (1) a step of producing a compound (A) having a urea linkage, using an organic primary amine having at least one primary amino group per molecule and at least one compound selected from among carbon dioxide and carbonic acid derivatives, at a temperature lower than the thermal dissociation temperature of the urea linkage; and(2) a step of reacting the compound (A) with a carbonate ester to produce a carbamate.

N - substituted carbamic acid ester

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Paragraph 0088; 0089; 0092, (2017/08/29)

PROBLEM TO BE SOLVED: To provide a method of manufacturing N-substituted carbamate ester with a high yield, a high purity and high efficiency (in a short time) without generation of byproducts.SOLUTION: A method of manufacturing N-substituted carbamate ester from an organic amine, urea and an aromatic hydroxy compound includes a process of supplying a composition containing a carbonic acid derivative and the aromatic hydroxy compound to a bottom part of a reaction apparatus where a synthetic reaction of the N-substituted carbamate ester occurs.

Using carbon dioxide diarylbutadiene isocyanate production method (by machine translation)

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Paragraph 0121, (2017/01/02)

PROBLEM TO BE SOLVED: To provide a method in which there are not various problems shown in a prior art when isocyanate is manufactured without using phosgene, and that can stably manufacture isocyanate for the long period of time in good yield. SOLUTION: The manufacturing method of isocyanate includes: a process in which diaryl carbonate and an amine compound are made to react in the presence of an aromatic hydroxy compound as a reaction solvent, thereby a reaction mixture that includes carbamic acid aryl having an aryl group originated from diaryl carbonate, an aromatic hydroxy compound originated from diaryl carbonate, and diaryl carbonate is obtained; a process in which the reaction mixture is transported to a thermal cracking reactor; and a process in which the carbamic acid aryl is subjected to a thermal decomposition reaction to obtain isocyanate, wherein a reactor in which the reaction of diaryl carbonate and an amine compound is performed and a thermal cracking reactor of carbamic acid aryl are different. COPYRIGHT: (C)2013,JPO&INPIT

Method for Producing Carbonyl Compund

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Paragraph 0653-0655, (2013/07/19)

A method for producing a carbonyl compound of the present invention comprises a step (X) of reacting a specific compound having a urea bond with a carbonic acid derivative having a carbonyl group (—C(═O)—) under heating at a temperature equal to or higher

PROCESS FOR PRODUCING ISOCYANATES USING DIARYL CARBONATE

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, (2011/04/14)

An object of the present invention is to provide a process that enables isocyanate to be produced stably over a long period of time and at high yield without encountering problems of the prior art during production of isocyanate without using phosgene. The present invention provides an isocyanate production process including the steps of: obtaining a reaction mixture containing an aryl carbamate having an aryl group originating in a diaryl carbonate, an aromatic hydroxy compound originating in a diaryl carbonate, and a diaryl carbonate, by reacting a diaryl carbonate and an amine compound in the presence of a reaction solvent in the form of an aromatic hydroxy compound; transferring the reaction mixture to a thermal decomposition reaction vessel; and obtaining isocyanate by applying the aryl carbamate to a thermal decomposition reaction, wherein the reaction vessel in which the reaction between the diaryl carbonate and the amine compound is carried out and the thermal decomposition reaction vessel for the aryl carbamate are different.

PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER

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, (2011/06/10)

The present invention provides a method for producing N-substituted carbamic acid-O-aryl ester derived from a compound having an ureido group, the method comprising the step of carrying out esterification or esterification and transesterification from the compound having the ureido group and a hydroxy composition containing one type or a plurality of types of hydroxy compounds.

PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE

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Page/Page column 45, (2011/02/18)

An object of the present invention is to provide a process that enables isocyanate to be produced stably over a long period of time and at high yield without encountering problems of the prior art during production of isocyanate without using phosgene. The present invention provides an isocyanate production process including the steps of: obtaining a reaction mixture containing an aryl carbamate having an aryl group originating in a diaryl carbonate, an aromatic hydroxy compound originating in a diaryl carbonate, and a diaryl carbonate, by reacting a diaryl carbonate and an amine compound in the presence of a reaction solvent in the form of an aromatic hydroxy compound; transferring the reaction mixture to a thermal decomposition reaction vessel; and obtaining isocyanate by applying the aryl carbamate to a thermal decomposition reaction, wherein the reaction vessel in which the reaction between the diaryl carbonate and the amine compound is carried out and the thermal decomposition reaction vessel for the aryl carbamate are different.

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