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175131-75-6

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175131-75-6 Usage

General Description

1,3-Cyclohexanediamine,2-methyl, (1alpha,2alpha,3alpha)-(9CI) is a chemical compound with the molecular formula C8H18N2. It is a derivative of cyclohexanediamine, and has a cyclic structure with a methyl group attached to the second carbon atom. 1,3-Cyclohexanediamine,2-methyl-,(1alpha,2alpha,3alpha)-(9CI) is primarily used as an intermediate in the production of various polymers, resins, and pharmaceuticals. It is also used as a curing agent for epoxy resins and as a building block for the synthesis of complex organic molecules. Additionally, 1,3-Cyclohexanediamine,2-methyl, (1alpha,2alpha,3alpha)-(9CI) has applications in the manufacturing of adhesives, coatings, and other materials. However, it is important to handle this chemical with care as it can potentially pose health hazards and environmental risks if not managed properly.

Check Digit Verification of cas no

The CAS Registry Mumber 175131-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175131-75:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*1)+(2*7)+(1*5)=126
126 % 10 = 6
So 175131-75-6 is a valid CAS Registry Number.

175131-75-6Upstream product

175131-75-6Downstream Products

175131-75-6Relevant articles and documents

Ru/g-C3N4as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines

Cao, Junya,Cao, Yan,Chen, Jiaqiang,Han, Fenggang,He, Peng,Huang, Xiaoyu,Li, Huiquan,Wang, Liguo,Yang, Huanhuan

, p. 16515 - 16525 (2020/05/13)

A series of Ru/g-C3N4materials with highly dispersed Ru were firstly prepared by an ultrasonic impregnation method using carbon nitride as a support. The catalysts were characterized by various techniques including BET and elemental analysis, ICP-AES, XPS, XRD, CO2-TPD and TEM. The results demonstrated that Ru/g-C3N4materials with a mesoporous structure and highly dispersed Ru were successfully prepared. The chemo-selective hydrogenation ofp-phenylenediamine (PPDA) to 1,4-cyclohexanediamine (CHDA) over Ru/g-C3N4as a model reaction was investigated in detail. PPDA conversion of 100% with a CHDA selectivity of more than 86% could be achieved under mild conditions. It can be inferred that the carbon nitride support possessed abundant basic sites and the Ru/g-C3N4-Tcatalysts provided suitable basicity for the aromatic ring hydrogenation. Compared to the N-free Ru/C catalyst, the involvement of nitrogen species in Ru/g-C3N4remarkably improved the catalytic performance. In addition, the recyclability of the catalyst demonstrated that the aggregation of Ru nanoparticles was responsible for the decrease of the catalytic activity. Furthermore, this strategy also could be expanded to the selective hydrogenation of other aromatic diamines to alicyclic diamines.

A method for the preparation of amine curing agent

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Paragraph 0023; 0024; 0028; 0029; 0030; 0031, (2017/04/29)

The invention discloses a preparation method of alicyclic amine curing agent. The method includes steps of dissolving methylphenylenediamine, as a raw material, in an organic solvent and performing a reaction with stirring for 5-12 hours in the presence o

Alicyclic amine curing agent for the preparation of

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Paragraph 0017; 0018; 0022-0025, (2017/12/27)

The invention discloses a preparation method of an alicyclic amine curing agent, which comprises the following steps: dissolving the raw material methyl phenylenediamine in an organic solvent; and in the presence of a supported metal catalyst, stirring to

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