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Cycloheptane, nitro-, also known as nitrocycloheptane, is a cyclic alkane with the molecular formula C7H13NO2. It consists of a seven-membered carbon ring with a nitro group (-NO2) attached to one of the carbon atoms. This organic compound is a derivative of cycloheptane, where one hydrogen atom is replaced by a nitro group. Nitrocycloheptane is an oily liquid with limited solubility in water and is used as a precursor in the synthesis of various pharmaceuticals, explosives, and other chemical compounds. Due to its reactivity and potential applications, it is essential to handle nitrocycloheptane with caution, as it can be hazardous and may pose health and environmental risks.

2562-40-5

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2562-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2562-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2562-40:
(6*2)+(5*5)+(4*6)+(3*2)+(2*4)+(1*0)=75
75 % 10 = 5
So 2562-40-5 is a valid CAS Registry Number.

2562-40-5SDS

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 nitrocycloheptane

1.2 Other means of identification

Product number -
Other names Nitro-cycloheptan

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:2562-40-5 SDS

2562-40-5Upstream product

2562-40-5Relevant academic research and scientific papers

Site-specific catalytic activities to facilitate solvent-free aerobic oxidation of cyclohexylamine to cyclohexanone oxime over highly efficient Nb-modified SBA-15 catalysts

Ding, Wei,Mao, Liqiu,Peng, Haoyu,Yin, Dulin,Zhong, Wenzhou

, p. 3409 - 3422 (2020/06/09)

The development of highly active and selective heterogeneous catalysts for efficient oxidation of cyclohexylamine to cyclohexanone oxime is a challenge associated with the highly sensitive nitrogen center of cyclohexylamine. In this work, dispersed Nb oxide supported on SBA-15 catalysts are disclosed to efficiently catalyze the selective oxidation of cyclohexylamine with high conversion (>75%) and selectivity (>84%) to cyclohexanone oxime by O2without any addition of solvent (TOF = 469.8 h?1, based on the molar amount of Nb sites). The role of the active-site structure identity in dictating the site-specific catalytic activities is probed with the help of different reaction and control conditions and multiple spectroscopy methods. Complementary to the experimental results, further poisoning tests (with KSCN or dehydroxylation reagents) and DFT computational studies clearly unveil that the surface exposed active centers toward activation of the reactants are quite different: the surface -OH groups can catch the NH2group from cyclohexylamine by forming a hydrogen bond and lead to a more facile cyclohexylamine oxidation to desired products, while the monomeric or oligomeric Nb sites with a highly distorted structure play a key role in the dissociation of O2molecules beneficial for insertion of active oxygen species into cyclohexylamine. These catalysts exhibit not only satisfactory recyclability for cyclohexylamine oxidation but also efficiently catalyze the aerobic oxidation of a wide range of amines under solvent-free conditions.

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