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118407-85-5

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118407-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118407-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,4,0 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118407-85:
(8*1)+(7*1)+(6*8)+(5*4)+(4*0)+(3*7)+(2*8)+(1*5)=125
125 % 10 = 5
So 118407-85-5 is a valid CAS Registry Number.

118407-85-5Downstream Products

118407-85-5Relevant academic research and scientific papers

Synthesis of: N -[(2-hydroxyethoxy)carbonyl]glycine from carbon dioxide, ethylene oxide, and α-amino acid by ionic gelation of sodium tripolyphosphate (TPP) and spirulina supported on magnetic KCC-1 in aqueous solution

Zhiani, Rahele,Khoobi, Mehdi,Sadeghzadeh, Seyed Mohsen

, p. 10153 - 10160 (2018/06/18)

In this study, a novel ionic gelation (IG) of sodium tripolyphosphate (TPP) and spirulina was prepared that, supported on magnetic fibrous silica nanospheres (Fe3O4/KCC-1/IG), has been developed for the synthesis of N-[(2-hydroxyetho

CO2 activation and fixation: highly efficient syntheses of hydroxy carbamates over Au/Fe2O3

Shang, Jianpeng,Guo, Xiaoguang,Li, Zuopeng,Deng, Youquan

, p. 3082 - 3088 (2016/06/06)

This paper reports an effective route for the syntheses of hydroxy carbamates from the reaction of CO2, epoxides and amines catalyzed by a Au/Fe2O3 catalyst. Under the optimized reaction conditions, various hydroxy carbamates were successfully synthesized with 92-98% isolated yields. The catalyst could be reused for several runs without deactivation. A plausible reaction mechanism was proposed by which the hydroxy carbamate was formed through an ammonium carbamate intermediate and the catalyst mainly promoted further nucleophilic addition between the epoxide and ammonium carbamate.

CELLULOSE ACYLATE FILM, NOVEL COMPOUND, POLARIZING PLATE AND LIQUID CRYSTAL DISPLAY DEVICE

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Paragraph 0448; 0449, (2015/12/30)

A cellulose acylate film, which includes a compound denoted by general formula (I) below, the equivalent U of which, calculated as a value obtained by dividing the molecular weight of the compound by the number of divalent linking groups denoted by —O—C(═

Rational investigations in the ring opening of cyclic carbonates by amines

Blain,Jean-Gerard,Auvergne,Benazet,Caillol,Andrioletti

supporting information, p. 4286 - 4291 (2014/10/16)

Non-isocyanate polyurethanes (NIPUs) constitute a promising alternative for more classical polyurethanes (PUs) as they may display mechanical properties that can match those of PUs and their synthesis does not involve the use of toxic isocyanates. Yet, because of the lower reactivity of carbonates versus isocyanates, the synthesis of NIPUs is not straightforward and generally requires the use of a catalyst. Recently, several groups have reported on the use of different ranges of catalysts for promoting the nucleophilic attack of the amine on the carbonate. However, many of these studies involve the use of highly reactive amine and/or carbonate proscribing a complete panorama of the potentialities of the reaction. Herein, we propose a rational study of the catalyzed aminolysis of four representative cyclic carbonates that reveals that the thiourea organocatalyst 1 outperforms in many aspects, classical inorganic or other organic catalysts. the Partner Organisations 2014.

Facile synthesis of 3-alkyl-5-methyloxazolidine-2,4-diones and N-lactoyl-N,N′-dialkylureas

Saliu, Francesco,Galliani, Guido,Orlandi, Marco,Rindone, Bruno,Tolppa, Eeva-Liisa,Suarez-Bertoa, Ricardo

experimental part, p. 956 - 962 (2011/04/26)

(Chemical Equation Presented) The reaction between aliphatic amines and propylene carbonate can be performed in solventless conditions under microwave irradiation, becoming nearly complete within 15 min of irradiation. Oxidation of the formed mixture of 2-hydroxyethylcarbamates gives 3,5-methylalkyl- oxazolidine-2,4-diones. These compounds can react further with aliphatic primary amines to give N-lactoylureas. Copyright Taylor & Francis Group, LLC.

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