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51934-41-9

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51934-41-9 Usage

Chemical Properties

Light Yellow Oil

Uses

Ethyl 4-iodobenzoate can be used in the synthesis of biphenyl derivatives via Negishi cross coupling with the intermediates of the type ArMg(tmp)·2LiCl (tmp = trimethylolpropane). It can also be used as a starting material in the synthesis of p-carbomethoxyphenylmagnesium bromide, a polyfunctional organometallic reagent that can be used as building block in the synthesis of complex target molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 51934-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51934-41:
(7*5)+(6*1)+(5*9)+(4*3)+(3*4)+(2*4)+(1*1)=119
119 % 10 = 9
So 51934-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9IO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2H2,1H3

51934-41-9 Well-known Company Product Price

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

  • (A14570)  Ethyl 4-iodobenzoate, 98%   

  • 51934-41-9

  • 10g

  • 396.0CNY

  • Detail
  • Alfa Aesar

  • (A14570)  Ethyl 4-iodobenzoate, 98%   

  • 51934-41-9

  • 50g

  • 1422.0CNY

  • Detail
  • Alfa Aesar

  • (A14570)  Ethyl 4-iodobenzoate, 98%   

  • 51934-41-9

  • 250g

  • 3830.0CNY

  • Detail

51934-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-iodobenzoate

1.2 Other means of identification

Product number -
Other names RARECHEM AL BI 0710

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:51934-41-9 SDS

51934-41-9Relevant articles and documents

The synthesis and characterisation of coordination and hydrogen-bonded networks based on 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoic acid

Bryant, MacGuire R.,Burrows, Andrew D.,Fitchett, Christopher M.,Hawes, Chris S.,Hunter, Sally O.,Keenan, Luke L.,Kelly, David J.,Kruger, Paul E.,Mahon, Mary F.,Richardson, Christopher

, p. 9269 - 9280 (2015)

The synthesis, structural and thermal characterisation of a number of coordination complexes featuring the N,O-heteroditopic ligand 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoate, HL are reported. The reaction of H2L with cobalt(II) and nickel(II) ni

Access to α,α-Difluoro-γ-amino Acids by Nickel-Catalyzed Reductive Aryldifluoroacetylation of N -Vinylacetamide

Zhao, Qing-Wei,Yang, Zhi-Fang,Fu, Xia-Ping,Zhang, Xingang

supporting information, p. 1565 - 1569 (2020/11/16)

A nickel-catalyzed reductive aryldifluoroacetylation of N -vinylacetamide with ethyl chloro(difluoro)acetate and aryl iodides is described. This chelating amide carbonyl group-assisted strategy provides rapid access to a variety of protected α,α-difluoro-γ-amino acids that might have potential applications in peptide chemistry and protein engineering. An advantage of this method is its synthetic simplicity, with no preparation of organometallic reagents.

Construction of Esters through Sulfuryl Fluoride (SO 2 F 2) Mediated Dehydrative Coupling of Carboxylic Acids with Alcohols at Room Temperature

Qin, Hua-Li,S Alharbi, Njud,Wang, Shi-Meng

, p. 3901 - 3907 (2019/10/11)

A facile method for the construction of esters through dehydrative coupling of carboxylic acids with alcohols is developed. The reactions are mediated by sulfuryl fluoride (SO 2 F 2) at room temperature and proceed with high efficiency. The method has several advantages including broad substrate scope, mild conditions, excellent functional group compatibility and affords high yields, even on gram scale.

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