Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-Iodo-5-Methylbenzaldehyde is a chemical compound characterized by the molecular formula C8H7IO. It presents as a pale yellow crystalline solid, distinguished by its strong, pungent odor. 2-lodo-5-Methylbenzaldehyde is recognized for its unique chemical structure and reactivity, which positions it as a significant building block in a variety of chemical and pharmaceutical applications.

1106813-84-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1106813-84-6 Structure
  • Basic information

    1. Product Name: 2-lodo-5-Methylbenzaldehyde
    2. Synonyms: 2-lodo-5-Methylbenzaldehyde;2-iodo-5-Methylbenzaldehyde
    3. CAS NO:1106813-84-6
    4. Molecular Formula: C8H7IO
    5. Molecular Weight: 246
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1106813-84-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 276.1±28.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.764±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-lodo-5-Methylbenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-lodo-5-Methylbenzaldehyde(1106813-84-6)
    11. EPA Substance Registry System: 2-lodo-5-Methylbenzaldehyde(1106813-84-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1106813-84-6(Hazardous Substances Data)

1106813-84-6 Usage

Uses

Used in Organic Synthesis:
2-Iodo-5-Methylbenzaldehyde is utilized as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to serve as a key component in the creation of complex organic molecules, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-Iodo-5-Methylbenzaldehyde is employed as an intermediate for the synthesis of pharmaceuticals. Its properties make it a valuable asset in the development of new drugs, potentially leading to innovative treatments and therapies.
Used in Research and Development:
2-lodo-5-Methylbenzaldehyde is also used in the research and development of new materials and chemical processes. Its reactivity and structural characteristics facilitate the exploration of novel chemical reactions and the creation of new chemical entities.
Used in Antimicrobial Applications:
2-Iodo-5-Methylbenzaldehyde has been studied for its potential antimicrobial properties. It is used as a compound of interest in the search for new antimicrobial agents, which could contribute to the development of effective treatments against resistant bacterial strains.
Used in Anticancer Research:
Furthermore, 2-Iodo-5-Methylbenzaldehyde has been investigated for its potential anticancer properties. It is used in biological and pharmacological research to explore its effects on cancer cells, with the aim of identifying new avenues for cancer treatment and therapy.

Check Digit Verification of cas no

The CAS Registry Mumber 1106813-84-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,6,8,1 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1106813-84:
(9*1)+(8*1)+(7*0)+(6*6)+(5*8)+(4*1)+(3*3)+(2*8)+(1*4)=126
126 % 10 = 6
So 1106813-84-6 is a valid CAS Registry Number.

1106813-84-6Downstream Products

1106813-84-6Relevant articles and documents

Monodentate Transient Directing Group-Assisted Palladium-Catalyzed Direct ortho-C-H Iodination of Benzaldehydes for Total Synthesis of Hernandial

Chen, Xuerong,La, Ming,Liu, Dandan,Zhang, Fang-Lin,Zhou, Yirong

supporting information, p. 9184 - 9188 (2021/11/30)

The first palladium-catalyzed direct o-C-H iodination of benzaldehydes was successfully developed with the assistance of commercially available 2,5-bis(trifluoromethyl)aniline as the optimal monodentate transient directing group (MonoTDG). Moderate to exc

Palladium-Catalyzed, Norbornene-Mediated, ortho-Amination ipso-Amidation: Sequential C-N Bond Formation

Whyte, Andrew,Olson, Maxwell E.,Lautens, Mark

, p. 345 - 348 (2018/01/27)

A palladium-catalyzed, norbornene-mediated ortho- and ipso-C-N bond-forming Catellani reaction is reported. This reaction proceeds through a sequential intermolecular amination followed by intramolecular cyclization of a tethered amide. The products, ortho-aminated dihydroquinolinones, were generated in moderate to good yields and are present in bioactive molecules. This work highlights the challenge of competing intra- vs intermolecular palladium-catalyzed processes.

Cu-Catalyzed Enantioselective Ring Opening of Cyclic Diaryliodoniums toward the Synthesis of Chiral Diarylmethanes

Li, Bin,Chao, Zengyin,Li, Chunyu,Gu, Zhenhua

, p. 9400 - 9403 (2018/07/30)

A Cu-catalyzed enantioselective desymmetrizing ring-opening reaction of six-membered cyclic diaryliodonium salts with carboxylic acids or thioacids is reported for the facile access to chiral diarylmethanes. A Cu/[cyclopropyl bis(oxazoline)] catalyst well

F- Nucleophilic-Addition-Induced [3 + 2] Annulation: Direct Access to CF3-Substituted Indenes

Tang, Hai-Jun,Zhang, Yu-Feng,Jiang, Yi-Wen,Feng, Chao

, p. 5190 - 5193 (2018/09/12)

An efficient [3 + 2] annulation of (2,2-difluorovinyl)-2-iodoarenes and internal alkynes was developed for the synthesis of 1-(trifluoromethyl)-1H-indenes. The success of this strategy hinges upon a well-balanced process for the generation of two transient reactive species, specifically trifluoroethylsilver and alkenylpalladium intermediates, in the same molecule, as well as a smooth transmetalation step, which delicately joins together these two different metallic intermediates.

Synthesis of Functionalized Alkylidene Indanes and Indanones through Tandem Phosphine-Palladium Catalysis

Fan, Yi Chiao,Kwon, Ohyun

, p. 2058 - 2061 (2015/05/20)

Densely functionalized alkylidene indanes and indanones can be prepared efficiently in one pot, in high yields with good stereoselectivities (in some cases exclusively the Z-isomer), through a route involving phosphine-catalyzed Michael addition followed

Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons

Ma, Weiwei,Fang, Jie,Ren, Jun,Wang, Zhongwen

, p. 4180 - 4183 (2015/09/15)

A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropane 1,1-diesters has been successfully developed. This supplies an efficient and conceptually new strategy for construction of bridged bicyclo[2.2.2]octane skeletons. This [3 + 3]IMCC could be run up to gram scale and from easily prepared starting materials. This [3 + 3]IMCC, together with our previously reported [3 + 2]IMCC strategy, can afford either the bicyclo[2.2.2]octane or bicyclo[3.2.1]octane skeletons from the similar starting materials by regulating the substituents on vinyl group.

Palladium-catalyzed insertion of N-tosylhydrazones for the synthesis of isoindolines

Zhou, Ping-Xin,Luo, Jian-Yi,Zhao, Lian-Biao,Ye, Yu-Ying,Liang, Yong-Min

, p. 3254 - 3256 (2013/05/08)

Isoindolines are synthesized by palladium-catalyzed coupling reaction of N-(2-iodobenzyl) anilines with α,β-unsaturated N-tosylhydrazones. The reaction has several potential advantages: (1) toleration of a wide range of functional groups, (2) easy to handle and with mild conditions, (3) enriches the isoindoline family, (4) two new bonds form in one step.

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 1106813-84-6