837408-71-6 Usage
General Description
4-Bromo-3-(ethoxymethyl)benzaldehyde is a chemical compound with the molecular formula C10H11BrO2. It is a brominated benzaldehyde derivative with an ethoxymethyl group attached to the aromatic ring. 4-BROMO-3-(ETHOXYMETHYL)BENZALDEHYDE is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also utilized as a reagent in organic chemistry, particularly in the preparation of various organic compounds. Additionally, 4-Bromo-3-(ethoxymethyl)benzaldehyde has potential applications in the fragrance and flavor industry. As with any chemical, it is important to handle and use this compound with proper safety precautions and in accordance with established protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 837408-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,7,4,0 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 837408-71:
(8*8)+(7*3)+(6*7)+(5*4)+(4*0)+(3*8)+(2*7)+(1*1)=186
186 % 10 = 6
So 837408-71-6 is a valid CAS Registry Number.
837408-71-6Relevant articles and documents
A BIPHENYLSULFONAMIDE ENDOTHELIN AND ANGIOTENSIN II RECEPTOR ANTAGONIST TO TREAT GLOMERULOSCLEROSIS
-
Paragraph 0042; 0167; 0150, (2017/07/06)
Methods of administering and pharmaceutical compositions of a biphenyl sulphonamide compound which is a dual angiotensin and endothelin receptor antagonist are disclosed for treating diseases.
Discovery of 4'-[(imidazol-1-yl)methyl]biphenyl-2-sulfonamides as dual endothelin/angiotensin II receptor antagonists.
Tellew, John E,Baska, Rose Ann F,Beyer, Sophie M,Carlson, Kenneth E,Cornelius, Lyndon A,Fadnis, Leena,Gu, Zhengxiang,Kunst, Bridgette L,Kowala, Mark C,Monshizadegan, Hossain,Murugesan, Natesan,Ryan, Carol S,Valentine, Maria T,Yang, Yifan,Macor, John E
, p. 1093 - 1096 (2007/10/03)
A series of 4'-[(imidazol-1-yl)methyl]biphenylsulfonamides has potent antagonist activity against both angiotensin II AT(1) and endothelin ET(A) receptors. Such dual-acting antagonists could have utility in the treatment of hypertension, heart failure, an