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91251-29-5

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91251-29-5 Usage

Description

1-(3',4'-DIMETHYLPHENYL)ETHYLAMINE is an organic amine with the molecular formula C11H17N. It features a phenyl ring with two methyl groups at the 3' and 4' positions, and an ethylamine functional group attached to the phenyl ring. This versatile compound serves as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, as well as a building block for new materials and research chemicals.

Uses

Used in Pharmaceutical Industry:
1-(3',4'-DIMETHYLPHENYL)ETHYLAMINE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and enhance their efficacy.
Used in Agrochemical Industry:
1-(3',4'-DIMETHYLPHENYL)ETHYLAMINE is used as an intermediate in the synthesis of agrochemicals to help create effective compounds for agricultural applications, such as pesticides and fertilizers.
Used in Organic Compounds Synthesis:
1-(3',4'-DIMETHYLPHENYL)ETHYLAMINE is used as a building block in the development of new organic compounds, contributing to the creation of innovative materials and chemical products.
Used in Material Development:
1-(3',4'-DIMETHYLPHENYL)ETHYLAMINE is used as a component in the research and development of new materials, potentially leading to advancements in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 91251-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,5 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91251-29:
(7*9)+(6*1)+(5*2)+(4*5)+(3*1)+(2*2)+(1*9)=115
115 % 10 = 5
So 91251-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N/c1-7-4-5-10(9(3)11)6-8(7)2/h4-6,9H,11H2,1-3H3

91251-29-5Upstream product

91251-29-5Downstream Products

91251-29-5Relevant articles and documents

The Synthesis of Primary Amines through Reductive Amination Employing an Iron Catalyst

B?umler, Christoph,Bauer, Christof,Kempe, Rhett

, p. 3110 - 3114 (2020/06/01)

The reductive amination of ketones and aldehydes by ammonia is a highly attractive method for the synthesis of primary amines. The use of catalysts, especially reusable catalysts, based on earth-abundant metals is similarly appealing. Here, the iron-catalyzed synthesis of primary amines through reductive amination was realized. A broad scope and a very good tolerance of functional groups were observed. Ketones, including purely aliphatic ones, aryl–alkyl, dialkyl, and heterocyclic, as well as aldehydes could be converted smoothly into their corresponding primary amines. In addition, the amination of pharmaceuticals, bioactive compounds, and natural products was demonstrated. Many functional groups, such as hydroxy, methoxy, dioxol, sulfonyl, and boronate ester substituents, were tolerated. The catalyst is easy to handle, selective, and reusable and ammonia dissolved in water could be employed as the nitrogen source. The key is the use of a specific Fe complex for the catalyst synthesis and an N-doped SiC material as catalyst support.

Triazine derivatives, a process for preparing the derivatives, and herbicides containing the derivatives as the effective component

-

, (2008/06/13)

A triazine derivative represented by the general formula: STR1 wherein R1 and R2 are each an alkyl group having 1 to 4 carbon atoms, and X1 and X2 are each a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, or an alkylthio group having 1 to 4 carbon atoms. This invention also provides a process for efficiently preparing said triazine derivative and a herbicide containing said triazine derivative as effective component.

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