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2,4-Dihydroxy-3-iodobenzaldehyde is a chemical compound with the molecular formula C7H5IO3. It is an organic compound bearing both hydroxyl and aldehyde functional groups, and it contains an iodine atom attached to the benzene ring. 2,4-Dihydroxy-3-iodobenzaldehyde has been studied for its potential use in organic synthesis and pharmaceutical applications.

82954-52-7

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82954-52-7 Usage

Uses

Used in Organic Synthesis:
2,4-Dihydroxy-3-iodobenzaldehyde is used as a building block for the synthesis of various organic compounds due to its reactivity and ability to undergo a range of chemical transformations.
Used in Pharmaceutical Applications:
2,4-Dihydroxy-3-iodobenzaldehyde is used as a potential candidate for pharmaceutical applications, given its potential biological activities, such as anti-inflammatory and antimicrobial properties. This makes it a promising compound for the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 82954-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,5 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82954-52:
(7*8)+(6*2)+(5*9)+(4*5)+(3*4)+(2*5)+(1*2)=157
157 % 10 = 7
So 82954-52-7 is a valid CAS Registry Number.

82954-52-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dihydroxy-3-iodobenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2,4-dihydroxy-3,5-dimethoxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82954-52-7 SDS

82954-52-7Downstream Products

82954-52-7Relevant academic research and scientific papers

1 -HYDROXY-BENZOOXABOROLES AS ANTIPARASITIC AGENTS

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Page/Page column 54; 106, (2014/10/03)

Provided are compounds useful for controlling endoparasites both in animals and agriculture. Further provided are methods for controlling endoparasite infestations of an animal by administering an effective amount of a compound as described above, or a pharmaceutically acceptable salt thereof, to an animal, as well as formulations for controlling endoparasite infestations using the compounds described above or an acceptable salt thereof, and an acceptable carrier. The claimed compounds are described by the following Markush formula:A typical example for a compound according to above formula is: A typical example for a compound according to above formula is:

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.

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