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2-(4-bromo-2-formyl-5-methoxyphenoxy)acetic acid is a complex organic compound characterized by its molecular formula C9H7BrO5. 2-(4-bromo-2-formyl-5-methoxyphenoxy)acetic acid features a 2-formyl (aldehyde) group, a 4-bromo substituent, and a 5-methoxy group attached to a phenoxy ring, which is connected to a 2-carbon acetic acid chain. The presence of the bromine atom and the formyl group suggests potential reactivity and functional group chemistry, making it a compound of interest in synthetic organic chemistry and potentially in the development of pharmaceuticals or other specialty chemicals. Its specific structure and properties could allow for a variety of applications, such as in the synthesis of more complex molecules or as a precursor in chemical reactions.

20073-16-9

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20073-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20073-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,7 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20073-16:
(7*2)+(6*0)+(5*0)+(4*7)+(3*3)+(2*1)+(1*6)=59
59 % 10 = 9
So 20073-16-9 is a valid CAS Registry Number.

20073-16-9Downstream Products

20073-16-9Relevant academic research and scientific papers

PYRIMIDINE DERIVATIVES AS PGE2 RECEPTOR MODULATORS

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Page/Page column 118, (2018/12/13)

The present invention relates to pyrimidine derivatives of formula (I) wherein (R1)n, R3, R4a, R4b, R5a, R5b and Ar1 are as described in the description and their use in the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor. The invention further relates to novel benzofurane and benzothiophene derivatives of formula (II) and their use as pharmaceuticals, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as modulators of the prostaglandin 2 receptors EP2 and/or EP4.

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