Welcome to LookChem.com Sign In|Join Free
  • or
2,3,5-Triiodo-benzoyl chloride is an organoiodine chemical compound with the molecular formula C7H2ClI3O. It is a yellowish solid that is highly reactive and can be hazardous if not handled properly. This versatile compound is commonly used in organic synthesis and as a reagent in the pharmaceutical industry, as well as in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It also serves as a building block for the preparation of other organic compounds. Due to its reactive nature and potential hazards, it should be handled and stored with caution and in accordance with proper safety protocols.

42860-33-3

Post Buying Request

42860-33-3 Suppliers

Recommended suppliers

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

42860-33-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3,5-Triiodo-benzoyl chloride is used as a reagent for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3,5-Triiodo-benzoyl chloride is used as a reagent in the synthesis of agrochemicals, which are essential for crop protection and enhancement of agricultural productivity.
Used in Dye Industry:
2,3,5-Triiodo-benzoyl chloride is used as a reagent in the synthesis of dyes, which are important for coloring fabrics, plastics, and other materials.
Used in Organic Synthesis:
As a versatile compound in organic chemistry, 2,3,5-Triiodo-benzoyl chloride is used as a building block for the preparation of other organic compounds, enabling the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 42860-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42860-33:
(7*4)+(6*2)+(5*8)+(4*6)+(3*0)+(2*3)+(1*3)=113
113 % 10 = 3
So 42860-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H2ClI3O/c8-7(12)4-1-3(9)2-5(10)6(4)11/h1-2H

42860-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-Triiodobenzoyl chloride

1.2 Other means of identification

Product number -
Other names 2,3,5-Triiodo-benzoyl chloride

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:42860-33-3 SDS

42860-33-3Relevant academic research and scientific papers

ONIUM SALT COMPOUND, CHEMICALLY AMPLIFIED RESIST COMPOSITION AND PATTERNING METHOD

-

Paragraph 0224-0225, (2021/06/21)

PROBLEM TO BE SOLVED: To provide a chemically amplified resist composition that has high sensitivity in photolithography using, as a light source, high energy rays such as KrF excimer laser light, ArF excimer laser light, electron beams, extreme ultraviol

RESIST COMPOSITION AND PATTERNING PROCESS

-

Paragraph 0204-0205, (2020/08/13)

A resist composition comprising a base polymer and a quencher in the form of an amine compound having an iodized aromatic ring bonded to the nitrogen atom via a divalent hydrocarbon group offers a high sensitivity and minimal LWR or improved CDU, independ

IODINE-CONTAINING PHOTOACID GENERATORS AND COMPOSITIONS COMPRISING THE SAME

-

Paragraph 0113, (2019/06/07)

A photoacid generator compound having formula (I): wherein, in formula (I), groups and variables are the same as described in the specification.

RESIST COMPOSITION AND PATTERNING PROCESS

-

Paragraph 0188-0189, (2019/12/25)

A resist composition comprising a base polymer and an onium salt of N-carbonylsulfonamide having iodized benzene ring offers a high sensitivity, minimal LWR and improved CDU, independent of whether it is of positive or negative tone.

Radiopaque poly(ε-caprolactone) as additive for X-ray imaging of temporary implantable medical devices

Samuel, Rémi,Girard, Edouard,Chagnon, Grégory,Dejean, Stéphane,Favier, Denis,Coudane, Jean,Nottelet, Benjamin

, p. 84125 - 84133 (2015/10/28)

Implantable polymeric medical devices suffer from a lack of visibility under current clinical imaging techniques. To circumvent this problem, poly(ε-caprolactone-co-α-triiodobenzoate-ε-caprolactone)s (PCL-TIB) containing from 3.5% to 24% of triiodobenzoat

RADIOPAQUE POLYMERS FOR MEDICAL DEVICES

-

Paragraph 00141, (2014/08/20)

Radiopaque polymer compositions and methods for making the compositions are provided. These radiopaque polymer compositions include polymer compositions comprising a crosslinked polymer network, the network comprising a first repeating unit derived from a

Organic radiographic contrasting agents for medical devices

-

Page/Page column 5, (2008/06/13)

The present invention discloses an organic radiographic contrasting agent containing an aliphatic or alicyclic backbone and multiple halogen-substituted aromatic groups. Each of the halogen-substituted aromatic groups in the radiographic contrasting agent

Synthesis and evaluation of potential CT (computer tomography) contrast agents for bone structure and microdamage analysis

Parkesh, Raman,Gowin, Wolfgang,Lee, T. Clive,Gunnlaugsson, Thorfinnur

, p. 3611 - 3617 (2008/09/19)

The design and synthesis of several novel X-ray contrast agents 1-3, developed for targeting bone structures, and in particularly microcracks in bones, using CT (Computer Tomography) detection is described. These contrast agents are based on the use of the well known triiodobenzene platform, which was conjugated into one or more phenyliminodiacetate moieties, which can be used to 'lock' onto bone matrices. Compounds 1-3 were all tested for their ability to visualise cracks in bone structures (bovine bones) using μ-CT imaging. The Royal Society of Chemistry 2006.

Synthesis and properties of radiopaque polymer hydrogels II: Copolymers of 2,4,6-triiodophenyl- or N-(3-carboxy-2,4,6-triiodophenyl)- acrylamide and p-styrene sulfonate

Okamura, Masahiko,Yamanobe, Takeshi,Arai, Tomohiro,Uehara, Hiroki,Komoto, Tadashi,Hosoi, Seiichi,Kumazaki, Tatsuo

, p. 17 - 28 (2007/10/03)

In order to pursue a possibility of application of radiopaque polymer hydrogels to vascular embolization, studies were made on synthesis of iodine containing copolyanions and properties of their hydrogels with polycation via formation of polyion complexes (PIC). Acrylamide derivatives having triiodophenyl groups were synthesized and copolymerized with sodium styrene sulfonate (SS) under several conditions. It was found that N-(3-carboxy-2,4,6-triiodophenyl)-acrylamide (CIPA) and 2,4,6-triiodophenylacrylamide (TIPA) monomers are effectively copolymerized with SS, while N-allyl-2,3,5-triiodobenzamide (ATIBA) are hardly copolymerized. Hydrogels were prepared by mixing aqueous solutions of polyanions, i.e. the copolymers (PCIPA and PTIPA) and polyallylamine (PAAn). 13C NMR spectra of PCIPA/PAAn and PTIPA/PAAn hydrogels gave peaks for both polyanion and polycation. This means that there remained free anionic and cationic monomer units, which did not form ion pairs because of spatial hindrance. Time dependence of 1H T2 showed quick increment and plateau for PSS/PAAn and gradual increments for PCIPA/PAAn. Therefore, PIC containing the radiopaque copolymer retains the hydrogel state for a long time. Embolization was examined by injection of PCIPA/PAAn hydrogels into the vein of a removed porcine kidney as a preliminary test for transcatheter arterial embolization (TAE). X-ray radiograms of the embolized organ were reasonably explained based on the structure and mobility of hydrogels.

X-ray opaque dental materials

-

, (2008/06/13)

X-ray opaque esters or amides of iodosubstituted benzoic acid according to formula I and polymers and dental materials produced therefrom. STR1 R1 =hydrogen or C1 to C3 alkyl, preferably H or CH3 ; R2 =straight-chain or branched C1 to C6 alkylene, oxyalkylene or arylene, preferably C2 to C4 alkylene and particularly preferably --CH2 --CH2 -- and --CH2 CH(--)CH2 --; X=O or NH, preferably O; R3 -R7 =at least 3 iodine substituents, preferably in R3, R4 and R6 or R3, R5 and R7 position, the other groups are hydrogen, C1 to C6 alkyl, C1 to C6 alkoxy, --Cl, --Br, --OH, --NH2, --N(C1 to C6 alkyl)2 or --NH--CO--(C1 to C6 alkyl), preferably R3, R4, and R6 are=I and R5 and R7 =H, or R3, R5 and R7 =I and R4 and R6 =--NH(COCH3); n=1, 2 or 3, preferably 1 or 2. The benzoic acid esters and amides according to the invention can be well polymerized radically or anionically, the polymers are well soluble in the usual dental monomers. Dental materials produced from the monomers or polymers are characterized in that the X-ray opaque component is bonded covalently into the polymeric matrix material and cannot therefore be washed out. Furthermore, excellent X-ray opacity can be achieved without using fillers.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 42860-33-3