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5-Iodo-2-Methylbenzaldehyde is an organic compound with the CAS number 1121-79-9. It is a derivative of benzaldehyde, featuring an iodine atom and a methyl group on the phenyl ring. This substance is an off-white to beige crystalline powder with a mild, aromatic scent. It is primarily used in the synthesis of other complex organic compounds, particularly in medicinal chemistry.

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  • 65874-26-2 Structure
  • Basic information

    1. Product Name: 5-iodo-2-Methylbenzaldehyde
    2. Synonyms: 5-iodo-2-Methylbenzaldehyde
    3. CAS NO:65874-26-2
    4. Molecular Formula: C8H7IO
    5. Molecular Weight: 246.04505
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65874-26-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 280.3±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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-iodo-2-Methylbenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-iodo-2-Methylbenzaldehyde(65874-26-2)
    11. EPA Substance Registry System: 5-iodo-2-Methylbenzaldehyde(65874-26-2)
  • 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: 65874-26-2(Hazardous Substances Data)

65874-26-2 Usage

Uses

Used in Medicinal Chemistry:
5-Iodo-2-Methylbenzaldehyde is used as a synthetic intermediate for the production of various complex organic compounds. It plays a crucial role in the development of new pharmaceuticals, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
5-Iodo-2-Methylbenzaldehyde is used as a reagent in the synthesis of other organic compounds. Its standard reactivity allows it to form Schiff bases with amines, which can be further utilized in the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 65874-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65874-26:
(7*6)+(6*5)+(5*8)+(4*7)+(3*4)+(2*2)+(1*6)=162
162 % 10 = 2
So 65874-26-2 is a valid CAS Registry Number.

65874-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Iodo-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:65874-26-2 SDS

65874-26-2Upstream product

65874-26-2Downstream Products

65874-26-2Relevant articles and documents

N-Iodosuccinimide (NIS) in Direct Aromatic Iodination

Bergstr?m, Maria,Suresh, Ganji,Naidu, Veluru Ramesh,Unelius, C. Rikard

, p. 3234 - 3239 (2017/06/21)

N-Iodosuccinimide (NIS) in pure trifluoroacetic acid (TFA) offers a time-efficient and general method for the iodination of a wide range of mono- and disubstituted benzenes at room temperature, as demonstrated in this paper. The starting materials were generally converted into mono-iodinated products in less than 16 hours at room temperature, without byproducts. A few deactivated substrates needed addition of sulfuric acid to increase the reaction rate. Another exception was methoxybenzenes that preferentially were iodinated by NIS in acetonitrile with only catalytic amounts of TFA.

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