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Butanoic acid, 2-(phenylmethylene)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88153-39-3

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88153-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88153-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,5 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88153-39:
(7*8)+(6*8)+(5*1)+(4*5)+(3*3)+(2*3)+(1*9)=153
153 % 10 = 3
So 88153-39-3 is a valid CAS Registry Number.

88153-39-3SDS

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 2-benzylidenebutanoic acid

1.2 Other means of identification

Product number -
Other names 2-Aethyl-3c-phenyl-acrylsaeure

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:88153-39-3 SDS

88153-39-3Downstream Products

88153-39-3Relevant academic research and scientific papers

Visible-light promoted oxidative cyclization of cinnamic acid derivatives using xanthone as the photocatalyst

Zhao, Bin,Xu, Bo

supporting information, p. 568 - 573 (2021/02/06)

We have developed an efficient photocatalytic synthesis of coumarin derivativesviaa tandem double bond isomerization/oxidative cyclization of cinnamic acids. Inexpensive and stable xanthone was used as the photocatalyst, and readily available Selectfluor was used as the oxidant. This method tolerates a wide range of functional groups and offers excellent chemical yields in general. Besides, the photocatalytic oxidative cyclization of cinnamic acid esters gives dimerized lignan-type products.

Copper-Catalyzed Stereodefined Construction of Acrylic Acid Derivatives from Terminal Alkynes via CO2 Insertion

Kuge, Kenta,Luo, Ying,Fujita, Yuki,Mori, Yasuyuki,Onodera, Gen,Kimura, Masanari

supporting information, p. 854 - 857 (2017/02/26)

IPrCuCl catalyzes the CO2 insertion reaction undergone by a dialkylvinylborane intermediate derived from alkynyltrialkylborate by a 1,2-alkyl group migration to afford α-alkyl acrylic acids with excellent regio- and stereoselectivities.

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