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5-HYDROXY-2-IODOBENZALDEHYDE is a chemical compound characterized by the molecular formula C7H5IO2. It is a yellow solid that exhibits limited solubility in water but is readily soluble in organic solvents. 5-HYDROXY-2-IODOBENZALDEHYDE serves as a versatile precursor in organic synthesis, playing a significant role in the creation of various chemical entities, particularly those with biological activity and pharmaceutical relevance.

50765-11-2

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50765-11-2 Usage

Uses

Used in Organic Synthesis:
5-HYDROXY-2-IODOBENZALDEHYDE is used as a precursor in organic synthesis for the production of a range of chemical compounds. Its unique structure allows it to be a key component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-HYDROXY-2-IODOBENZALDEHYDE is utilized as a starting material for the development of biologically active compounds. Its potential to contribute to the creation of new drugs makes it a valuable asset in medicinal chemistry.
Used in Material Science for Electronic Devices:
5-HYDROXY-2-IODOBENZALDEHYDE has been studied for its potential applications in material science, particularly for the development of materials used in electronic devices. Its properties may contribute to advancements in this field.
Used in Other Industrial Applications:
Beyond the realms of organic synthesis and pharmaceuticals, 5-HYDROXY-2-IODOBENZALDEHYDE also finds use in various other industrial applications where its chemical properties are beneficial.
It is crucial to handle 5-HYDROXY-2-IODOBENZALDEHYDE with care due to its potential health hazards if not used properly, emphasizing the need for safety measures during its manipulation and application.

Check Digit Verification of cas no

The CAS Registry Mumber 50765-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50765-11:
(7*5)+(6*0)+(5*7)+(4*6)+(3*5)+(2*1)+(1*1)=112
112 % 10 = 2
So 50765-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5IO2/c8-7-2-1-6(10)3-5(7)4-9/h1-4,10H

50765-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxy-2-iodobenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-hydroxy-2-iodobenzaldehyde

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:50765-11-2 SDS

50765-11-2Relevant academic research and scientific papers

INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE - SYNTHESIS AND USE THEREOF FOR TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA AND LYMPHOMA

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Page/Page column 24-25, (2021/05/07)

The present invention relates to new compounds of general formula I, their synthesis, their pharmaceutically acceptable salts, and their use in treatment of T-cell acute lymphoblastic leukemia and lymphoma.

Stereoselective synthesis of a: Podophyllum lignan core by intramolecular reductive nickel-catalysis

Xiao, Jian,Cong, Xiao-Wei,Yang, Gui-Zhen,Wang, Ya-Wen,Peng, Yu

supporting information, p. 2040 - 2043 (2018/03/01)

A Ni-catalyzed reductive cascade to a diastereocontrolled construction of THN[2,3-c]furan, is developed. The mild reaction conditions led to the tolerance of broad functional groups that can be placed in almost every position of this skeleton with good yields. The conformational control for the observed trans- or cis-fused selectivity during this tandem cyclization-coupling is also proposed.

ALKYNE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS

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Page/Page column 70, (2016/05/02)

Provided are compounds of formula (Ia) and pharmaceutically acceptable salts thereof, wherein A, B, R 1, R 2, m and n are as defined herein, which are active as inhibitors of S-Nitrosoglutathione reductase (GSNOR). These compounds prevent, inhibit, or suppress the action of GSNOR and are therefore useful in the treatment of GSNOR mediated diseases, disorders, syndromes or conditions such as, e.g., pulmonary hypertension, acute respiratory distress syndrome (ARDS), asthma, bronchospasm, cough, pneumonia, pulmonary fibrosis, interstitial lung diseases, cystic fibrosis and chronic obstructive pulmonary disease (COPD).

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