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"N,N'-(4,4'-methanediyl-di-phenyl)-bis-carbamic acid dipropyl ester" is a complex organic compound with the chemical formula C22H28N2O4. It is a bis-carbamic acid ester derivative, characterized by a central methanediyl-di-phenyl bridge connecting two carbamic acid moieties. The carbamic acid groups are esterified with propyl groups, resulting in a molecule that is part of a class of compounds known for their potential applications in various chemical and pharmaceutical processes. N,N'-(4,4'-methanediyl-di-phenyl)-bis-carbamic acid dipropyl ester is also referred to as a urethane or a carbamate ester, indicating its structural features and functional groups. It is important to note that handling and use of such chemicals require appropriate safety measures due to their potential reactivity and toxicity.

60483-67-2

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60483-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60483-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60483-67:
(7*6)+(6*0)+(5*4)+(4*8)+(3*3)+(2*6)+(1*7)=122
122 % 10 = 2
So 60483-67-2 is a valid CAS Registry Number.

60483-67-2Downstream Products

60483-67-2Relevant academic research and scientific papers

Development of solvent-free synthesis of hydrogen-bonded supramolecular polyurethanes

Houton, Kelly. A.,Burslem, George M.,Wilson, Andrew. J.

, p. 2382 - 2388 (2015)

In this work we describe the solvent free synthesis of supramolecular polyurethanes held together by heterocomplementary triple hydrogen bonding. We perform a systematic evaluation on the base catalyzed synthesis of small molecule ureas and carbamates fro

Novel material forming supramolecular structures, process and uses

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Page/Page column 11-12, (2008/12/08)

The invention relates to novel material, forming supramolecular structures below its transition temperature, which contains at least one C=O and/or C=S group and at least one N—H, O—H and/or S—H group and wherein the material has the structure [in-line-formulae]A(—X—B)n ??(1)[/in-line-formulae] wherein A is a cyclic, aromatic and/or aliphatic group, n being a number of 1 to 4, —X—B is, if n is 2, the same or different, and if n is 3 or 4, the same, partly the same or different and has one of the structures (2) to (4) [in-line-formulae]NH—C(Y)—Y—B ??(2)[/in-line-formulae] [in-line-formulae]—NH—C(Y)—NR—B ??(3)[/in-line-formulae] [in-line-formulae]—Y—C(Y)—NR—B ??(4)[/in-line-formulae] with Y being an Oxygen and/or Sulfur atom, B being an organic group with at least one heteroatom, where the heteroatom is bound to at least two carbon atoms when B is linear or cyclic, and where the heteroatom is bound to at least one carbon atom when B is branched, and R being a Hydrogen atom, a cyclic, aromatic and/or aliphatic group or another B group which is the same or different. The material can be made by reacting at least one isocyanate and/or thioisocyanate with at least one amine, alcohol and/or thiol. Typically, the material is used first below its transition temperature, followed by increasing the temperature to around or above the transition temperature, carrying out a process step and subsequently decrease the temperature below the transition temperature.

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