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157942-12-6

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157942-12-6 Usage

Uses

Useful intermediate for pharmaceutical and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 157942-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,9,4 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157942-12:
(8*1)+(7*5)+(6*7)+(5*9)+(4*4)+(3*2)+(2*1)+(1*2)=156
156 % 10 = 6
So 157942-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7IO3/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4,10H,1H3

157942-12-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H64354)  Methyl 3-hydroxy-4-iodobenzoate, 97%   

  • 157942-12-6

  • 250mg

  • 326.0CNY

  • Detail
  • Alfa Aesar

  • (H64354)  Methyl 3-hydroxy-4-iodobenzoate, 97%   

  • 157942-12-6

  • 1g

  • 980.0CNY

  • Detail
  • Alfa Aesar

  • (H64354)  Methyl 3-hydroxy-4-iodobenzoate, 97%   

  • 157942-12-6

  • 5g

  • 3920.0CNY

  • Detail

157942-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-hydroxy-4-iodobenzoate

1.2 Other means of identification

Product number -
Other names 3-hydroxy-4-iodo-benzoic acid methyl ester

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:157942-12-6 SDS

157942-12-6Relevant articles and documents

Zinc(II)-Assisted Aryl Finkelstein Reaction for the Synthesis of Aryl Iodides

Ueberschaar, Nico,Heine, Daniel,Hertweck, Christan

, p. 1794 - 1797 (2016)

Aryl iodides play an important role in synthetic organic chemistry as they are frequently utilized in cross-coupling reactions and in oxidation processes using hypervalent iodine compounds. Their synthesis is, however, often cumbersome and may lead to unwanted side products. Here, we report on an improved protocol for the aryl Finkelstein reaction in which dehalogenation is prevented by addition of zinc iodide in lieu of copper(I). Generally, electron-poor ortho-bromo methyl benzoates, amides, and even unprotected phenols are well-suited for this method.

Total synthesis of polymorphatin A, a macrocyclic bisbibenzyl with boat configured arenes

Almalki, Faisal A.,Sun, Wei,Light, Mark E.,Harrowven, David C.

, (2020/09/04)

Polymorphatin A was reported as a constituent of Marchantia polymorpha in 2007 following much speculation as to its likely existence as a natural product. Interest was rekindled when a claimed total synthesis revealed inconsistencies in spectral data betw

STILBENE AND FUSED STILBENE DERIVATIVES AS SOLAR CELL DYES

-

Paragraph 00162; 00163, (2018/12/02)

The present application discloses stilbene derivative compounds and phenyl- benzofuran compositions, useful in the manufacture of dye-sensitized solar cells and other similar technology.

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