149244-04-2 Usage
Structure
Benzene ring, featuring an allyloxy group and an azidomethyl group as substituents.
Allyloxy group
An allyl group (C3H5) attached to an oxygen atom (C=C-O-).
Azidomethyl group
A methyl group (CH3) connected to three azide groups (N3).
Synthesis applications
Utilized in organic synthesis for modifying and functionalizing various molecules.
Polymer and material preparation
Can be employed in the production of polymers and materials with specific chemical and physical properties.
Reactivity
The presence of the azidomethyl group makes the compound potentially reactive, which may lead to various applications.
Organic photochemistry
The compound may have applications in the field of organic photochemistry due to its reactivity.
Precursor for synthesis
1-allyloxy-2-azidomethylbenzene can serve as a precursor for the synthesis of other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 149244-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,4 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149244-04:
(8*1)+(7*4)+(6*9)+(5*2)+(4*4)+(3*4)+(2*0)+(1*4)=132
132 % 10 = 2
So 149244-04-2 is a valid CAS Registry Number.
149244-04-2Relevant academic research and scientific papers
Steric acceleration of intramolecular cycloaddition reactions
Orlek, Barry S.,Sammes, Peter G.,Weller, David J.
, p. 8179 - 8194 (2007/10/02)
Use of conformational constraints, induced by different ortho-substituents in 1-allyloxy-2-(substituted)methylbenzenes, where the substituent is a 1,3-dipole such as the azide or 3-oxidopyridinium group, can be employed to accelerate the 1,3-dipolar cycloaddition reaction. In this manner cycloadditions that otherwise do not proceed can be forced to react.
