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34633-09-5

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34633-09-5 Usage

General Description

4-Iodocinnamic acid is a chemical compound with the molecular formula C9H7IO2. It is a derivative of cinnamic acid and contains a carboxylic acid functional group and an iodine atom. It is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various compounds. Its properties and structure make it a versatile compound in the field of medicinal chemistry, where it is used as a starting material for the synthesis of potential drug candidates. Additionally, its ability to undergo various chemical reactions makes it a valuable intermediate in the production of fine chemicals and specialty products.

Check Digit Verification of cas no

The CAS Registry Mumber 34633-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34633-09:
(7*3)+(6*4)+(5*6)+(4*3)+(3*3)+(2*0)+(1*9)=105
105 % 10 = 5
So 34633-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H7IO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6H,(H,11,12)/b6-3+

34633-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-iodophenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names p-IODOCINNAMIC ACID

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:34633-09-5 SDS

34633-09-5Relevant articles and documents

Radical-Cation Vinylcyclopropane Rearrangements by TiO2Photocatalysis

Maeta, Naoya,Kamiya, Hidehiro,Okada, Yohei

supporting information, p. 6551 - 6566 (2020/07/14)

Radical cation vinylcyclopropane rearrangements by TiO2 photocatalysis in lithium perchlorate/nitromethane solution are described. The reactions are triggered by oxidative single electron transfer, which is followed by immediate ring-opening of the cyclopropanes to generate distonic radical cations as unique reactive intermediates. This approach can also be applied to vinylcyclobutane, leading to the construction of six-membered rings. A stepwise mechanism via distonic radical cations is proposed based on preliminary mechanistic studies, which is supported by density functional theory calculations.

An electroluminescent compound and an electroluminescent device comprising the same

-

Paragraph 0328-0331, (2016/10/10)

The present invention relates to an organic light emitting compound adopted to an organic electroluminescent device. The organic light emitting compound is represented by chemical formula 1. In the case of adopting the same as a dopant compound in a lumin

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