68050-88-4 Usage
Structure
1,3,5-Cycloheptatriene-1-carboxaldehyde, 6-ethenyl
Explanation
The structure describes the arrangement of atoms in the molecule. It consists of a cycloheptatriene ring with a carboxaldehyde group (-CHO) attached to the 1-carbon and an ethenyl group (-CH=CH2) attached to the 6-carbon.
Explanation
The compound is derived from cycloheptatriene, which is a seven-carbon ring with alternating double and single bonds.
Explanation
The compound contains two functional groups a carboxaldehyde group (-CHO) at the 1-carbon and an ethenyl group (-CH=CH2) at the 6-carbon.
Explanation
1,3,5-Cycloheptatriene-1-carboxaldehyde, 6-ethenyl(9CI) is used in organic synthesis, which involves the formation of new chemical compounds from simpler molecules.
6. Research and Industrial Applications
Explanation
The compound may have certain hazardous properties, which can pose health risks if not handled properly. It is important to follow safety guidelines and precautions when working with this chemical.
Explanation
Due to its potential hazardous properties, it is crucial to handle 1,3,5-Cycloheptatriene-1-carboxaldehyde, 6-ethenyl(9CI) with caution, using appropriate safety equipment and following proper disposal methods.
Aldehyde Derivative
Cycloheptatriene
Functional Groups
Carboxaldehyde and Ethenyl
Applications
Organic Synthesis
Hazardous Properties
Potential Health Risks
Handling Precautions
Caution Required
Check Digit Verification of cas no
The CAS Registry Mumber 68050-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,5 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68050-88:
(7*6)+(6*8)+(5*0)+(4*5)+(3*0)+(2*8)+(1*8)=134
134 % 10 = 4
So 68050-88-4 is a valid CAS Registry Number.
68050-88-4Relevant academic research and scientific papers
Klingensmith, Kenneth A.,Puettmann, Wilhelm,Vogel, Emanuel,Michi, Josef
, p. 3375 - 3380 (1983)
Eight 2-substituted and nine 3-substituted 1,6-methanoannulenes have been synthesized, and their magnetic circular dichroism has been measured.The B terms of the Lb transition depend on the ?-electron effect of the substituent in a way which reveals the ordering of the four frontier molecular orbitals: a1, a2, b1, and b2 in the order of increasing energy.This result implies the presence of a strong transannular interaction between the bridgehead positions 1 and 6 on the bridged annulene ring.
