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16004-15-2

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16004-15-2 Usage

Chemical Properties

light yellow adhering crystalline powder

Uses

4-Iodobenzyl bromide is used as an organic chemical synthesis intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 16004-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,0 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16004-15:
(7*1)+(6*6)+(5*0)+(4*0)+(3*4)+(2*1)+(1*5)=62
62 % 10 = 2
So 16004-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrI/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2

16004-15-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A18200)  4-Iodobenzyl bromide, 97%   

  • 16004-15-2

  • 5g

  • 931.0CNY

  • Detail
  • Alfa Aesar

  • (A18200)  4-Iodobenzyl bromide, 97%   

  • 16004-15-2

  • 25g

  • 3943.0CNY

  • Detail
  • Alfa Aesar

  • (A18200)  4-Iodobenzyl bromide, 97%   

  • 16004-15-2

  • 100g

  • 12855.0CNY

  • Detail

16004-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodobenzyl Bromide

1.2 Other means of identification

Product number -
Other names 1-(bromomethyl)-4-iodobenzene

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:16004-15-2 SDS

16004-15-2Relevant articles and documents

Ethyl 2-formamido-2-(4-iodobenzyl)-3-(4-iodophenyl)propionate and ethyl 2-(3-bromobenzyl)-3-(3-bromophenyl)-2-formamidopropionate

Damodharan, Lakshminarasimhan,Pattabhi, Vasantha,Behera, Manoranjan,Kotha, Sambasivarao

, p. o216-o218 (2003)

The title compounds, C19H19I2NO3 and C19H19Br2NO3, are derivatives of α-aminoisobutyric acid with halogen substituents at the para and meta positions, respectively. The ethoxycarbonyl and formamide side chains attached to the Cαatom of the molecule adopt extended and folded conformations, respectively. The crystal structures are stabilized by N -H...O, C - H...O, C - Br...O and C - I...O interactions.

Halogenation through Deoxygenation of Alcohols and Aldehydes

Chen, Jia,Lin, Jin-Hong,Xiao, Ji-Chang

supporting information, p. 3061 - 3064 (2018/05/28)

An efficient reagent system, Ph3P/XCH2CH2X (X = Cl, Br, or I), was very effective for the deoxygenative halogenation (including fluorination) of alcohols (including tertiary alcohols) and aldehydes. The easily available 1,2-dihaloethanes were used as key reagents and halogen sources. The use of (EtO)3P instead of Ph3P could also realize deoxy-halogenation, allowing for a convenient purification process, as the byproduct (EtO)3Pa?O could be removed by aqueous washing. The mild reaction conditions, wide substrate scope, and wide availability of 1,2-dihaloethanes make this protocol attractive for the synthesis of halogenated compounds.

A General Strategy to Enhance the Performance of Dye-Sensitized Solar Cells by Incorporating a Light-Harvesting Dye with a Hydrophobic Polydiacetylene Electrolyte-Blocking Layer

Desta, Mekonnen Abebayehu,Liao, Chia-Wei,Sun, Shih-Sheng

, p. 690 - 697 (2017/03/22)

A unique strategy to suppress charge recombination effectively and enhance light harvesting in dye-sensitized solar cells (DSSCs) is demonstrated by the design of a new dipolar organic dye functionalized with a diacetylene unit, which is capable of underg

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