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Tricyclic[3.2.1.0~3,6~]octane, also known as tricyclo[3.2.1.0^3,6]octane, is a cyclic hydrocarbon compound with a unique molecular structure. It consists of three fused rings, with the central ring being a cyclopropane ring, and the two outer rings being cyclohexane rings. The compound has a molecular formula of C8H12 and is an example of a polycyclic aromatic hydrocarbon (PAH). Tricyclo[3.2.1.0^3,6]octane is a colorless, crystalline solid with a melting point of 47-48°C. It is insoluble in water but soluble in organic solvents such as ethanol and acetone. Due to its complex structure, it has limited industrial applications, but it is of interest to chemists for its unique properties and potential use in the synthesis of other compounds.

250-22-6

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250-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250-22-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250-22:
(5*2)+(4*5)+(3*0)+(2*2)+(1*2)=36
36 % 10 = 6
So 250-22-6 is a valid CAS Registry Number.

250-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 250-22-6

1.2 Other means of identification

Product number -
Other names Tricyclo<3.2.1.03.6>octan

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:250-22-6 SDS

250-22-6Downstream Products

250-22-6Relevant academic research and scientific papers

Synthesis and Bridgehead Reactivities of 1-Substituted Tricyclo3,6>octanes

Luh, Tien-Yau,Lei, Keng Lon

, p. 5328 - 5331 (2007/10/02)

Ten bridgehead 1-substituted tricyclo3,6>octanes were conveniently synthesized by our newly developed route.Thus, 5-allyl-5-(carboethoxy)cyclopentenone was irradiated to give a mixture of the tricyclic keto esters 5a and 5b, which were converted to 1-(carboethoxy)tricyclo3,6>octane by the reduction of the corresponding thioketals.The ester function was then transformed to various substituents.The pKa of the bridgehead carboxylic acid was determined.The bridgehead radical reactivity was also examined.The results were compared with those of the related systems.

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