131088-03-4 Usage
Description
2,4-dihydroxy-5-iodobenzaldehyde is a chemical compound with the molecular formula C7H5IO3. It is a yellow crystalline solid that features two hydroxyl groups and one iodine atom attached to a benzene ring, along with an aldehyde functional group. 2,4-dihydroxy-5-iodobenzaldehyde is utilized in the synthesis of various organic compounds and has demonstrated moderate antibacterial and antifungal activities.
Uses
Used in Organic Synthesis:
2,4-dihydroxy-5-iodobenzaldehyde is used as a reagent in organic synthesis for the creation of different organic compounds. Its unique structure, which includes hydroxyl and iodine atoms, makes it a valuable intermediate in chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,4-dihydroxy-5-iodobenzaldehyde is used as a starting material for the production of various pharmaceuticals. Its properties allow it to be a key component in the development of new drugs.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 2,4-dihydroxy-5-iodobenzaldehyde is employed as a starting material for the synthesis of various agrochemicals. Its moderate antibacterial and antifungal activities make it suitable for use in products designed to protect crops and enhance agricultural yields.
Used in Antibacterial and Antifungal Applications:
2,4-dihydroxy-5-iodobenzaldehyde is used as an active ingredient in antibacterial and antifungal products due to its reported moderate activities against these microorganisms, contributing to the development of treatments and preventive measures in both medical and agricultural contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 131088-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,8 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 131088-03:
(8*1)+(7*3)+(6*1)+(5*0)+(4*8)+(3*8)+(2*0)+(1*3)=94
94 % 10 = 4
So 131088-03-4 is a valid CAS Registry Number.
131088-03-4Relevant articles and documents
MOLECULES PRESENTING DUAL EMISSION PROPERTIES
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Page/Page column 30, (2016/02/09)
The present invention concerns compound of formula (I): wherein: - A represents an electron-withdrawing group; - D represents an electron-donating group; - X is selected from the group consisting of: O, S and NR, wherein R is selected from the group consi
Facile synthesis of natural moracin compounds using PD(OAC)2/P(TBU)3-HBF4 as a sonogashira coupling reagent
Lee, Jae Jun,Yun, So-Ra,Jun, Jong-Gab
, p. 3453 - 3458 (2015/02/02)
An efficient and practical synthesis of natural moracins, which have diverse range of biological properties including anticancer, antioxidant, and antibacterial activities, has been achieved using Pd(OAc)2/P(tBu)3-HBF
The first total synthesis of moracin O and moracin P, and establishment of the absolute configuration of moracin O
Kaur, Navneet,Xia, Yan,Jin, Yinglan,Dat, Nguyen Tien,Gajulapati, Kondaji,Choi, Yongseok,Hong, Young-Soo,Lee, Jung Joon,Lee, Kyeong
supporting information; experimental part, p. 1879 - 1881 (2009/10/23)
The first total synthesis of the naturally occurring benzofurans, moracins O and P was achieved using a Sonogashira cross coupling reaction followed by in situ cyclization, and the absolute configuration of natural moracin O was established.