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(2-methyl-6-nitrophenyl)methanamine is an organic compound that belongs to the class of amines. It is a derivative of methanamine, with a methyl and nitro group attached to a phenyl ring. The chemical structure of (2-methyl-6-nitrophenyl)methanamine includes a nitrogen atom bonded to two hydrogen atoms and a benzene ring. It can be used as a building block in the synthesis of various pharmaceuticals or other organic compounds due to its unique structure and reactivity. The nitro group in (2-methyl-6-nitrophenyl)methanamine can impart specific properties and functionalities to the molecule, making it useful in various chemical and industrial applications.

131780-95-5

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131780-95-5 Usage

Uses

Used in Pharmaceutical Industry:
(2-methyl-6-nitrophenyl)methanamine is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity. The presence of the nitro group can impart specific properties and functionalities to the molecule, making it useful in the development of new drugs.
Used in Chemical Industry:
(2-methyl-6-nitrophenyl)methanamine is used as a chemical intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the production of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 131780-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131780-95:
(8*1)+(7*3)+(6*1)+(5*7)+(4*8)+(3*0)+(2*9)+(1*5)=125
125 % 10 = 5
So 131780-95-5 is a valid CAS Registry Number.

131780-95-5Upstream product

131780-95-5Downstream Products

131780-95-5Relevant academic research and scientific papers

A dual site catalyst for mild, selective nitrile reduction

Lu, Zhiyao,Williams, Travis J.

, p. 5391 - 5393 (2014)

We report a novel ruthenium bis(pyrazolyl)borate scaffold that enables cooperative reduction reactivity in which boron and ruthenium centers work in concert to effect selective nitrile reduction. The pre-catalyst compound [κ3-(1-pz)2HB(N = CHCH3)]Ru(cymene) + TfO- (pz = pyrazolyl) was synthesized using readily-available materials through a straightforward route, thus making it an appealing catalyst for a number of reactions. the Partner Organisations 2014.

DUAL SITE CATALYST FOR MILD, SELECTIVE NITRILE REDUCTION

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Paragraph 0052, (2016/06/09)

A ruthenium bis(pyrazolyl)borate scaffold that enables cooperative reduction reactivity in which boron and ruthenium centers work in concert to effect selective nitrile reduction is provided. The pre-catalyst compound [κ3-(1-pz)2HB(N═CHCH3)]Ru(cymene)? TfO? (pz=pyrazolyl) was synthesized using readily-available materials through a straightforward route, thus making it an appealing catalyst for a number of reactions.

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