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1213827-87-2

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1213827-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1213827-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,8,2 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1213827-87:
(9*1)+(8*2)+(7*1)+(6*3)+(5*8)+(4*2)+(3*7)+(2*8)+(1*7)=142
142 % 10 = 2
So 1213827-87-2 is a valid CAS Registry Number.

1213827-87-2Relevant articles and documents

Production of Adipic Acid from Sugar Beet Residue by Combined Biological and Chemical Catalysis

Zhang, Hongfang,Li, Xiukai,Su, Xiaoyun,Ang, Ee Lui,Zhang, Yugen,Zhao, Huimin

, p. 1500 - 1506 (2016)

Adipic acid is one of the most important industrial dicarboxylic acids and is used mainly as a precursor to nylon-6,6. Currently, commercial adipic acid is produced primarily from benzene by a chemical route that is associated with environmental, health, and safety concerns. Herein, we report a new process to produce adipic acid from an inexpensive renewable feedstock, sugar beet residue by combining an engineered Escherichia coli strain and Re-based chemical catalysts. The engineered E.coli converted d-galacturonic acid to mucic acid, which was precipitated easily with acid, and the mucic acid was further converted to adipic acid by a deoxydehydration reaction catalyzed by an oxorhenium complex followed by a Pt/C-catalyzed hydrogenation reaction under mild conditions. A high selectivity to the free acid products was achieved by tuning the acidity of the Re-based catalysts. Finally, adipic acid was produced directly from sugar beet residue that was hydrolyzed enzymatically with engineered E.coli and two chemical catalysts in a yield of 8.4 %, which signifies a new route for the production of adipic acid.

Kinetic and mechanistic investigation of oxidation of uronic acids by sodium N-bromoarylsulfonamides in alkaline medium

Shashikala,Rangappa

, p. 491 - 499 (2002)

The kinetics of oxidation of uronic acids (UAs), D-glucuronic acid and D-galacturonic acid, by sodium N-bromo-p-toluenesulfonamide or bromamine-T (BAT) and sodium N-bromobenzenesulfonamide or bromamine-B (BAB) in alkaline medium at 30°C have been investigated and the rate law, rate=k [OX] [UA] [HO-] where [OX][BAT] or [BAB] was observed. The product p-toluenesulfonamide (PTS) or benzenesulfonamide (BSA) and ionic strength have no influence on the rate. The rate decreased when the dielectric constant (ε) of the medium was decreased. The rate increased in D2O medium. Proton inventory studies were made in D2O-H2O mixtures. Effect of temperature was studied and from the Arrhenius plots, activation parameters were computed. A mechanism involving the formation of enediol anion, which reacts with positive bromine of the bromamine in the rate-limiting step is suggested.

Ehrlich

, p. 199 (1917)

Blakemore et al.

, p. 558 (1966)

Farrant et al.

, p. 161,164 (1971)

-

Posternak

, p. 1007,1009 (1936)

-

Lamiaceae carbohydrates. 1. Pectinic substances and hemicelluloses from Mentha x piperita

Olennikov,Tankhaeva

, p. 501 - 507 (2007)

Pectinic substances from the aerial part of Mentha x piperita were isolated and characterized and found to be a mixture of β-(1→4)-glucogalactan (MPG) and two α-(1→4)-rhamnopolygalacturonans (MPP'-1 and MPP'-2). It was shown that the pectin and its components exhibited membrane-stabilizing, antiatherogenic, and antioxidant activity. Hemicelluloses from M. piperita were a lignocarbohydrate complex.

Kinetics and mechanism of the oxidation of uronic acdis by sodium N-chlorobenzenesulphonamide in alkaline medium

Rangappa,Raghavendra,Mahadevappa

, p. 359 - 371 (1997)

The kinetics of oxidation of D-glucuronic acid and D-galacturonic acid (UA) by sodium N-chlorobenzenesulphonamide or chloramine-B (CAB) in alkaline medium at 35°C has been investigated and the rate law, rate = k [CAB][UA][HO-] was observed. The product, benzenesulphonamide had no influence. Increase of ionic strength increased the rate and when the dielectric constant of the medium was decreased, the rate was decreased. The rate increased in D2O medium and the inverse solvent isotope effect k (D2O)/k (H2O) was 2.00. Proton inventory was studied for the reactions in H2O-D2O mixtures. Activation parameters have been determined from the Arrhenius plots. The mechanism assumes the formation of an enediol anion followed by its oxidation by the positive halogen in a rate limiting step.

PROCESSES FOR PREPARING ALDARIC, ALDONIC, AND URONIC ACIDS

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Paragraph 0132-0143, (2021/05/29)

Various processes for preparing aldaric acids, aldonic acids, uronic acids, and/or lactone(s) thereof are described. For example, processes for preparing a C5-C6 aldaric acid and/or lactone(s) thereof by the catalytic oxidation of a C5-C6 aldonic acid and/or lactone(s) thereof and/or a C5-C6 aldose are described.

Novel synthetic process of mucic acid

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Paragraph 0035-0037; 0067, (2017/06/10)

The present invention relates to a method of synthesizing mucic acid from galactose derived from biomass including marine resources, and more specifically, to a method of synthesizing mucic acid which utilizes galactose as a starting material and through a chemical reaction, induces an oxidation reaction to synthesize mucic acid. The method of the present invention can easily synthesize mucic acid in a high yield from galactose and the like under low temperature and atmospheric pressure operating conditions, can be used as an intermediate to produce bio adipic acid, the raw material of nylon 66 that is used as a material for automobile parts, and, therefore, has high industrial applicability.(AA) Marine bio sugar mixture obtained after saccharification using non-food marine resources (galactose, or a mixture of galactose, glucose and rhamnose)(BB) Mixing of aqueous nitric acid solution with sugar mixture(CC) Oxidation reaction of bio sugar under low temperature condition (-15~0anddeg;C)(DD) Washing of solid products produced from chemical reaction and extraction of high-purity mucic acid particles using aqueous solution, having mucic acid dissolved therein, prepared in advanceCOPYRIGHT KIPO 2017

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