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Tricyclic[3.3.1.03,7]nonane, also known as tricyclo[3.3.1.03,7]nonane, is a cyclic hydrocarbon compound with a molecular formula of C9H16. It consists of three fused cycloalkane rings, specifically a cyclopropane, cyclobutane, and cyclohexane ring. Tricyclo[3.3.1.03,7]nonane is an example of a polycyclic aromatic hydrocarbon (PAH) and is known for its unique structure and potential applications in various chemical and industrial processes. Due to its complex structure, tricyclo[3.3.1.03,7]nonane is not commonly found in nature but can be synthesized in laboratories for research purposes.

7075-86-7

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7075-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7075-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7075-86:
(6*7)+(5*0)+(4*7)+(3*5)+(2*8)+(1*6)=107
107 % 10 = 7
So 7075-86-7 is a valid CAS Registry Number.

7075-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Tricyclo[3.3.1.03,7]nonane

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo[1,2-a][1,4]diazepine,octahydro

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:7075-86-7 SDS

7075-86-7Downstream Products

7075-86-7Relevant academic research and scientific papers

Decarbonylation of Adamantan-2-one by Two-photonic Excitation with XeCl Laser

Ichinose, Nobuyuki,Kawanishi, Shunichi

, p. 2017 - 2018 (2007/10/02)

Adamantan-2-one 1 in cyclohexane undergoes decarbonylation to give noradamantane 2 via two-photon absorption of XeCl laser light (308 nm).

Organic Peroxides, XIV. The Thermal Decomposition of Polycyclic tert-Butyl Bridgehead Peroxycarboxylates

Ruechardt, Christoph,Golzke, Volker,Range, Guenter

, p. 2769 - 2785 (2007/10/02)

Eleven bridgehead peresters (1, 2, 5 - 8, 10, 12, 14, 18, 21) have been prepared for the first time and the products and the kinetics of their thermal decomposition were investigated.The correlations of all known thermolysis constants of bridgehead peresters with the steric substituent constants φf, with the solvolysis constants of the corresponding bridgehead bromides, as well as with the change in strain enthalpy ΔHsp for hydride abstraction from the bridgehead, as calculated by the procedure of v.R.Schleyer, were analysed.The thermolysis constants of these peresters are mainly determined by the polar effect in the transition state of the perester fragmentation.

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