102613-41-2 Usage
Organic compound
A compound containing carbon atoms, which is the basis for 1-methoxy-3-naphthalen-1-ylurea's structure.
Naphthalene ring
A fused ring structure of two benzene rings found in 1-methoxy-3-naphthalen-1-ylurea, contributing to its chemical and physical properties.
Urea group
A functional group (-NH2)2CO, present in 1-methoxy-3-naphthalen-1-ylurea, which is responsible for its chemical reactivity and potential applications.
Intermediate in pharmaceutical synthesis
1-methoxy-3-naphthalen-1-ylurea is commonly used as an intermediate in the production of pharmaceuticals, helping to create more complex and effective drug molecules.
Potential use as pesticide/insecticide
This chemical may have applications as a pesticide or insecticide due to its effects on certain organisms, although its specific uses have not been extensively studied.
Solid at room temperature
1-methoxy-3-naphthalen-1-ylurea is a solid with a white to off-white color, indicating its physical state and appearance under standard conditions.
Safety precautions required
Researchers and handlers should use proper safety measures when working with 1-methoxy-3-naphthalen-1-ylurea, as its potential hazards and health effects have not been fully characterized.
Check Digit Verification of cas no
The CAS Registry Mumber 102613-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102613-41:
(8*1)+(7*0)+(6*2)+(5*6)+(4*1)+(3*3)+(2*4)+(1*1)=72
72 % 10 = 2
So 102613-41-2 is a valid CAS Registry Number.
102613-41-2Relevant articles and documents
Investigating N-methoxy-N′-aryl ureas in oxidative C-H olefination reactions: An unexpected oxidation behaviour
Willwacher, Jens,Rakshit, Souvik,Glorius, Frank
supporting information; experimental part, p. 4736 - 4740 (2011/08/06)
Herein, we report a urea derived directing group for mild and highly selective oxidative C-H bond olefination. Subsequent intramolecular Michael addition affords dihydroquinazolinones in good yields. The N-O bond of the urea substrate exhibits superior oxidative behaviour compared to a variety of other external oxidants. The Royal Society of Chemistry 2011.
