Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-Iodo-5-hydroxypyridine, with the CAS number 129034-38-4, is an organic compound characterized by its off-white powder appearance. It is primarily utilized in the field of organic synthesis, where it serves as a valuable building block for the creation of various complex molecules and pharmaceuticals.

129034-38-4

Post Buying Request

129034-38-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

129034-38-4 Usage

Uses

Used in Organic Synthesis:
2-Iodo-5-hydroxypyridine is used as a synthetic building block for the development of complex organic molecules and pharmaceuticals. Its unique chemical structure, featuring both an iodine atom and a hydroxyl group, allows for versatile reactivity and functional group manipulation in synthetic processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Iodo-5-hydroxypyridine is used as a key intermediate in the synthesis of various therapeutic agents. Its presence in the molecular structure can contribute to the desired biological activity and pharmacological properties of the final drug product.
Used in Chemical Research:
2-Iodo-5-hydroxypyridine is also employed in chemical research as a model compound to study the reactivity and properties of pyridine derivatives. This helps researchers gain insights into the behavior of similar compounds and develop new synthetic strategies or applications in various fields.

Synthesis Reference(s)

The Journal of Organic Chemistry, 62, p. 3008, 1997 DOI: 10.1021/jo970062g

Check Digit Verification of cas no

The CAS Registry Mumber 129034-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129034-38:
(8*1)+(7*2)+(6*9)+(5*0)+(4*3)+(3*4)+(2*3)+(1*8)=114
114 % 10 = 4
So 129034-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H4INO/c6-5-2-1-4(8)3-7-5/h1-3,8H

129034-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-5-Hydroxypyridine

1.2 Other means of identification

Product number -
Other names 6-Iodopyridin-3-ol

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:129034-38-4 SDS

129034-38-4Relevant articles and documents

BRM TARGETING COMPOUNDS AND ASSOCIATED METHODS OF USE

-

, (2019/10/23)

The present disclosure relates to bifunctional compounds, which find utility as modulators of SMARCA2 or BRM (target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a ligand that binds to the Von Hippel-Lindau E3 ubiquitin ligase, and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.

Synthesis and polarized photoluminescence of novel phosphorescent cyclometalated platinum dimer

Jiang, Shi Ping,Luo, Kai Jun,Wang, Ying Han,Wang, Xin,Jiang, Ying,Wei, Yan Yan

scheme or table, p. 1005 - 1008 (2012/01/11)

A novel phosphorescent cyclometalated platinum dimer with bis-[2-(p-dodecyloxyphenyl) pyridyl]-hexane-1,6-diol as ligand and 1,3-(1-n-hexyl,3-n-heptadecyl) diketone as ancillary ligand was synthesized. The chemical structure and liquid crystal property of

A revised synthesis of the antitumour antibiotic L-azatyrosine via 2-iodo-5-methoxypyridine

Seton, Alison W.,Stevens, Malcolm F. G.,Westwell, Andrew D.

, p. 546 - 548 (2007/10/03)

A revised synthesis of the antitumour antibiotic L-azatyrosine is reported, the main features of which are the unambiguous synthesis of the previously misinterpreted 2-iodo-5-methoxypyridine and subsequent palladium-catalysed coupling with an iodoalanine-derived zinc reagent.

Compounds and compositions as anticoagulants

-

, (2008/06/13)

The present invention relates to novel biheterocyclic derivatives which are factor Xa inhibitors; the pharmaceutically acceptable salts and N-oxides thereof; their uses as therapeutic agents and the methods of their making.

New water-soluble duocarmycin derivatives: Synthesis and antitumor activity of A-ring pyrrole compounds bearing β-heteroarylacryloyl groups

Amishiro, Nobuyoshi,Nagamura, Satoru,Kobayashi, Eiji,Gomi, Katsushige,Saito, Hiromitsu

, p. 669 - 676 (2007/10/03)

A series of A-ring pyrrole compounds of duocarmycin bearing 4'-methoxy- β-heteroarylacryloyl groups were synthesized and evaluated for in vitro anticellular activity against HeLa S3 cells and in vivo antitumor activity against murine sarcoma 18

DC-89 derivatives

-

, (2008/06/13)

Provided are DC-89 derivatives represented by the formula: STR1 wherein X represents Cl or Br, R represents hydrogen or COR1, and W represents STR2 and pharmaceutically acceptable salts thereof. The compounds of the present invention have excellent anti-tumor activity and are useful as anti-tumor agents.

An Efficient and Selective Method for the Preparation of Iodophenols

Edgar, Kevin J.,Falling, Stephen N.

, p. 5287 - 5291 (2007/10/02)

Direct iodination of a wide range of phenols may be achieved with unprecedented selectivity in aqueous alcohol solvents by the action of a reagent preparated in situ from sodium hypochlorite and sodium iodide.Para-substituted phenols (or ortho-substituted, when the para-position is already occupied) are obtained in fair to excellent yields by simple isolation techniques.The extent of iodination is easily controlled by stoichiometry.The technique is also useful with some anilines.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 129034-38-4