35367-34-1 Usage
Molecular Weight
310.28 g/mol
Structure
The compound has a benzene ring with two fluorine atoms at the 2 and 6 positions, a carbamoyl group (-CO-NH2) attached to the nitrogen atom, and a 4-(1-methylethyl)phenyl group attached to the amide carbonyl group.
+ Appearance
White crystalline solid
+ Melting Point
Not provided in the material
+ Solubility
Not provided in the material
+ Reactivity
The compound may undergo reactions that are typical for benzamide derivatives, such as hydrolysis, acylation, and amide bond formation or cleavage.
+ Stability
The compound is likely stable under normal conditions, but may decompose upon exposure to heat, light, or other forms of energy.
Biological Activity
The specific biological activity of 2,6-difluoro-N-[4-(1-methylethyl)phenyl]carbamoylbenzamide is not provided in the material, but it is commonly used in pharmaceutical research for the development of potential drug candidates.
Applications
The compound is used in medicinal chemistry and pharmacology for studying biological activity and drug interactions within the human body.
Check Digit Verification of cas no
The CAS Registry Mumber 35367-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,6 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35367-34:
(7*3)+(6*5)+(5*3)+(4*6)+(3*7)+(2*3)+(1*4)=121
121 % 10 = 1
So 35367-34-1 is a valid CAS Registry Number.
35367-34-1Relevant articles and documents
Enhancement of seed yield of soybeans by a substituted benzoyl urea
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, (2008/06/13)
A method is disclosed for increasing yield in soybeams by applying, in the absence of insect pressure on the crop, an amount effective for increasing seed pod formation of an active amount of a substituted benzoyl urea represented by structural formula (I).
