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2-BROMO-4-IODOBENZALDEHYDE, with the chemical formula C7H4BrIO, is a derivative of benzaldehyde featuring bromine and iodine atoms substituted at the 2 and 4 positions, respectively. 2-BROMO-4-IODOBENZALDEHYDE is known for its reactivity and is typically used in the synthesis of pharmaceuticals and agrochemicals, as well as in organic synthesis for constructing complex molecules. Careful handling and use in a well-ventilated area are recommended due to its reactive properties.

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  • 261903-03-1 Structure
  • Basic information

    1. Product Name: 2-BROMO-4-IODOBENZALDEHYDE
    2. Synonyms: 2-BROMO-4-IODOBENZALDEHYDE;Benzaldehyde, 2-broMo-4-iodo-
    3. CAS NO:261903-03-1
    4. Molecular Formula: C7H4BrIO
    5. Molecular Weight: 310.91
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261903-03-1.mol
  • Chemical Properties

    1. Melting Point: 112-114 ºC
    2. Boiling Point: 312.984 °C at 760 mmHg
    3. Flash Point: 143.088 °C
    4. Appearance: /
    5. Density: 2.231
    6. Vapor Pressure: 0.001mmHg at 25°C
    7. Refractive Index: 1.696
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-BROMO-4-IODOBENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BROMO-4-IODOBENZALDEHYDE(261903-03-1)
    12. EPA Substance Registry System: 2-BROMO-4-IODOBENZALDEHYDE(261903-03-1)
  • 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: 261903-03-1(Hazardous Substances Data)

261903-03-1 Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-4-IODOBENZALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex molecular structures that are essential in drug development.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 2-BROMO-4-IODOBENZALDEHYDE serves as an intermediate, playing a crucial role in the creation of compounds that are used in agricultural applications to protect crops and enhance yields.
Used in Organic Synthesis:
2-BROMO-4-IODOBENZALDEHYDE is utilized as a reagent in organic synthesis, particularly for the construction of complex molecules. Its unique substitution pattern allows for versatile reactions that are valuable in the synthesis of specialty chemicals and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 261903-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,9,0 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 261903-03:
(8*2)+(7*6)+(6*1)+(5*9)+(4*0)+(3*3)+(2*0)+(1*3)=121
121 % 10 = 1
So 261903-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrIO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H

261903-03-1SDS

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-BROMO-4-IODOBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names WT1557

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:261903-03-1 SDS

261903-03-1Relevant articles and documents

Synthesis and spectroscopic study of silacyclyne-substituted phenyleneethynylenes

Mao, Guoliang,Orita, Akihiro,Matsuo, Daisuke,Hirate, Takayoshi,Iwanaga, Tetsuo,Toyota, Shinji,Otera, Junzo

supporting information; experimental part, p. 2860 - 2864 (2009/09/06)

A series of 1,1-dimethyl-4,5:8,9-dibenzo-1-silacycloundeca-4,8-diene-2,6,10-triyne (DST)-substituted phenyleneethynylenes were successfully synthesized by reaction of Me2SiCl2 with dimagnesium dianions which had been prepared from 2,

A High-Spin and Durable Polyradical: Poly(4-diphenylaminium-1,2-phenylenevinylene)

Murata, Hidenori,Takahashi, Masahiro,Namba, Kazuaki,Takahashi, Naoki,Nishide, Hiroyuki

, p. 631 - 638 (2007/10/03)

A purely organic, high-spin, and durable polyradical molecule was synthesized: It is based on the non-Kekule- and non-disjoint design of a φ-conjugated poly(1,2-phenylenevinylene) backbone pendantly 4-substituted with multiple robust arylaminium radicals. 4-N,N-Bis(4-methoxy- and -tert-butylphenyl)amino-2-bromostyrene 5 were synthesized and polymerized with a palladium-phosphine catalyst to afford the head-to-tail-linked polyradical precursors (1). Oxidation of 1 with the nitrosonium ion solubilized with a crown ether gave the aminium polyradicals (1+) which were durable (half-life > 1 month) at room temperature in air. A high-spin ground state with an average S = (4.5)/2 for 1a+ was proved even at room temperature by magnetic susceptibility, magnetization, ESR, and NMR measurements.

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