91335-51-2 Usage
Description
2-BROMO-4,5-DIETHOXYBENZALDEHYDE, with the molecular formula C11H13BrO3, is a white to light yellow crystalline powder characterized by a strong odor. This chemical compound serves as a versatile building block in the synthesis of various organic compounds and pharmaceutical intermediates, as well as a reagent in chemical reactions. Its unique chemical properties have garnered interest in fields such as medicine, agriculture, and material science.
Uses
Used in Pharmaceutical Industry:
2-BROMO-4,5-DIETHOXYBENZALDEHYDE is used as a pharmaceutical intermediate for the synthesis of various medicinal compounds. Its unique structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the chemical industry, 2-BROMO-4,5-DIETHOXYBENZALDEHYDE is used as a reagent in chemical reactions, contributing to the production of a wide range of organic compounds.
Used in Material Science:
2-BROMO-4,5-DIETHOXYBENZALDEHYDE is utilized as a building block in the development of new materials, taking advantage of its unique chemical properties to create innovative products with specific characteristics.
Used in Agricultural Applications:
In agriculture, 2-BROMO-4,5-DIETHOXYBENZALDEHYDE may be employed in the synthesis of agrochemicals or as a component in the development of new pesticides or fertilizers.
It is crucial to handle 2-BROMO-4,5-DIETHOXYBENZALDEHYDE with care due to its potential health and environmental risks. Proper safety measures should be implemented during its use and disposal to mitigate any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 91335-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91335-51:
(7*9)+(6*1)+(5*3)+(4*3)+(3*5)+(2*5)+(1*1)=122
122 % 10 = 2
So 91335-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13BrO3/c1-3-14-10-5-8(7-13)9(12)6-11(10)15-4-2/h5-7H,3-4H2,1-2H3
91335-51-2Relevant articles and documents
Exquisite synthesis of a designed PAR-1 antagonist
Miao, Hua-Ming,Zhao, Gui-Long,Zhang, Lin-Shan,Shao, Hua,Wang, Jian-Wu
, p. 1981 - 1993 (2012/01/04)
The synthesis of a designed, sterically congested geminal dimethyl-bearing PAR-1 antagonist was achieved by a route of ten steps, with the oxidation of an electron-rich benzaldehyde, the construction of a tertiary alkyl azide, and the selective hydrogenolysis of a 1,5-fused tetrazole to generate the cyclic amidine with Raney-Ni being the key steps. The selective hydrogenolysis of 1,5-fused tetrazole to generate the cyclic amidine with Raney-Ni was discovered and may be generally used for the synthesis of structurally unusual cyclic amidines. Several unsuccessful attempts to construct the desired geminal dimethyl-bearing cyclic amidine were also discussed. Copyright