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51282-48-5

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51282-48-5 Usage

Description

2-Furancarboximidic acid, methyl ester, also known as Furan-2-carboximidic acid, is a heterocyclic organic compound with the molecular formula C6H7NO3. It is a derivative of furan and is commonly used as a precursor or intermediate in the synthesis of pharmaceuticals and agrochemicals. The methyl ester form of 2-Furancarboximidic acid is known for its potential use as a building block in organic chemistry and for its ability to react with various reagents to produce a wide range of compounds.

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Furancarboximidic acid, methyl ester is used as a precursor or intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its ability to react with different reagents makes it a valuable compound in the development of new drugs and pesticides.
Used in Perfume and Flavoring Industries:
2-Furancarboximidic acid, methyl ester is used as a building block in the production of perfumes and flavorings. Its versatility in reacting with various reagents allows for the creation of unique and complex scents and tastes.
Used in Polymer and Resin Manufacturing:
2-Furancarboximidic acid, methyl ester is used in the manufacturing of polymers and resins. Its ability to form a wide range of compounds makes it a useful component in the production of various types of plastics and resins.
Used in Antimicrobial Applications:
2-Furancarboximidic acid, methyl ester is known for its antimicrobial properties, making it a valuable compound in various industrial and medical applications. Its ability to inhibit the growth of microorganisms can be utilized in the development of disinfectants, sanitizers, and other antimicrobial products.

Check Digit Verification of cas no

The CAS Registry Mumber 51282-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,8 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51282-48:
(7*5)+(6*1)+(5*2)+(4*8)+(3*2)+(2*4)+(1*8)=105
105 % 10 = 5
So 51282-48-5 is a valid CAS Registry Number.

51282-48-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl furan-2-carboximidate

1.2 Other means of identification

Product number -
Other names methyl 2-furancarboximidate

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:51282-48-5 SDS

51282-48-5Relevant articles and documents

Alkali α-MnO2/Na: XMnO2 collaboratively catalyzed ammoxidation-Pinner tandem reaction of aldehydes

Jia, Xiuquan,Ma, Jiping,Wang, Min,Li, Xiaofang,Gao, Jin,Xu, Jie

, p. 7429 - 7436 (2016)

The tandem reaction is a growing field to yield important advances toward green and sustainable chemistry. Herein, we report a bifunctional manganese oxide catalyst with an interface binding redox phase (α-MnO2) and a basic phase (NaxMnO2). The molar ratio of NaOH/Mn plays a great role in the formation of α-MnO2/NaxMnO2. The sodium cation is essential for the formation of a basic NaxMnO2 phase while the potassium cation promotes the formation of a redox-active α-MnO2 phase. The interface structure of α-MnO2/NaxMnO2 geometrically favors the ammoxidation-Pinner tandem reaction to synthesize imidates in a 58-96% yield from aldehydes. Thus a phase collaborative effect is observed. In the ammoxidation process, the redox cycle of MnIV/MnIII is involved and the lattice oxygen in the α-MnO2 phase acts as an active oxygen species. The O-H in methanol is activated and dissociated on the basic sites of NaxMnO2 to the adsorbed methoxyl species to facilitate the Pinner synthesis. This approach bypasses the conventional synthesis of imidates, which suffer from harsh reaction conditions and the requirement for multiple steps.

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