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1829-28-3

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1829-28-3 Usage

Description

ETHYL 2-IODOBENZOATE is an organic compound with the chemical structure of an ethyl ester derivative of 2-iodobenzoic acid. It is characterized by its potential applications in various industries due to its unique properties.

Uses

Used in Pharmaceutical Industry:
ETHYL 2-IODOBENZOATE is used as an anti-infective agent for treating various infections. Its iodine content contributes to its effectiveness in combating harmful microorganisms and promoting overall health.
Used in Reproductive Health:
In the field of reproductive health, ETHYL 2-IODOBENZOATE serves as a contraceptive agent, helping to prevent unintended pregnancies by interfering with the reproductive process.
Used in Diagnostic Radiology:
ETHYL 2-IODOBENZOATE is also utilized as an x-ray contrast medium in diagnostic radiology. Its high atomic number and density allow for better visualization of internal structures during imaging procedures, aiding in the accurate diagnosis of various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1829-28-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1829-28:
(6*1)+(5*8)+(4*2)+(3*9)+(2*2)+(1*8)=93
93 % 10 = 3
So 1829-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9IO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6H,2H2,1H3

1829-28-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L07650)  Ethyl 2-iodobenzoate, 98%   

  • 1829-28-3

  • 5g

  • 414.0CNY

  • Detail
  • Alfa Aesar

  • (L07650)  Ethyl 2-iodobenzoate, 98%   

  • 1829-28-3

  • 25g

  • 1527.0CNY

  • Detail

1829-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 2-IODOBENZOATE

1.2 Other means of identification

Product number -
Other names ethyl 2-iodanylbenzoate

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:1829-28-3 SDS

1829-28-3Relevant articles and documents

Synthesis of E-stilbene azomethines as potent antimicrobial and antioxidant agents

Iqbal, Ahsan,Khan, Zulfiqar Ali,Shahzad, Sohail Anjum,Usman, Muhammad,Khan, Shakeel Ahmad,Fauq, Abdul H.,Bari, Ayesha,Sajid, Muhammad Aamir

, p. 1518 - 1533 (2018)

A series of new extensively conjugated E -stilbene azomethines (5a–5h) were synthesized and screened for their antioxidant and antimicrobial activity. The compounds were tested against bacterial (Escherichia coli, Staphylococcus aureus, Klebsiella pneumon

Synthesis and antiproliferative activity of substituted benzopyranoisoindoles: A new class of cytotoxic compounds

Hadjipavlou, Christiana,Kostakis, Ioannis K.,Pouli, Nicole,Marakos, Panagiotis,Pratsinis, Harris,Kletsas, Dimitris

, p. 4822 - 4825 (2006)

A series of novel aminosubstituted benzopyranoisoindoles possessing structural analogy to an active nitracrine metabolite are reported. The compounds exhibited interesting cytotoxic activity against a panel of cell lines, which was maximized by the presen

Synthesis, modeling studies and evaluation of E-stilbene hydrazides as potent anticancer agents

Iqbal, Ahsan,Khan, Zulfiqar Ali,Shahzad, Sohail Anjum,Ahmad Khan, Shakeel,Raza Naqvi, Syed Ali,Bari, Ayesha,Amjad, Hira,Umar, Muhammad Ihtisham

, p. 271 - 281 (2019)

A group of new thermodynamically more stable E-2-styrylbenzohydrazide derivatives (5a-i) were synthesized via palladium catalyzed Mizoroki-Heck reaction conditions. All synthesized compounds were characterized by UV-visible, FT-IR, 1H NMR, sup

Ynoate-Initiated Selective C-N Esterification of Tertiary Amines under Transition-Metal and Oxidant-Free Conditions

Sun, Feixiang,Feng, Huangdi,Huang, Liliang,Huang, Junhai

supporting information, p. 713 - 717 (2021/01/14)

An efficient and selective method for metal-and oxidant-free deaminated esterification of tertiary amines is presented. In this protocol, ynoates play a key role to activate the Csp 3-N bond through a process of in situ generation of zwitterionic salts. The transformations show that Csp 3-N bond in the zwitterionic species has a lower dissociation energy than Csp 2-N bond, leading to break preferentially and be trapped by carboxylic acids to generate the corresponding products in moderate to good yield.

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