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2-Propenoic acid, 3-[2-(1,3-dioxolan-2-yl)phenyl]-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91388-28-2

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91388-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91388-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,8 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91388-28:
(7*9)+(6*1)+(5*3)+(4*8)+(3*8)+(2*2)+(1*8)=152
152 % 10 = 2
So 91388-28-2 is a valid CAS Registry Number.

91388-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propenoic acid, 3-[2-(1,3-dioxolan-2-yl)phenyl]-, ethyl ester, (E)-

1.2 Other means of identification

Product number -
Other names -

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:91388-28-2 SDS

91388-28-2Relevant academic research and scientific papers

Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction

Qian, Hui,Zhao, Wanxiang,Sung, Herman H-Y.,Williams, Ian D.,Sun, Jianwei

supporting information, p. 4361 - 4363 (2013/06/05)

An efficient organocatalyzed strategy for the synthesis of 3-amino-1-indanols has been developed. This method is complementary to the conventional Friedel-Crafts strategy. It is also applicable to the synthesis of enantioenriched 3-amino-1-indanols.

1,7-Electrocyclisation and Carbene Reactions of o-Alkenylaryldiazoalkanes: The Effect of Alkene Configuration on the Mode of Reaction

Munro, David P.,Sharp, John T.

, p. 849 - 858 (2007/10/02)

The 1,7-8?-electron electrocyclisation of o-alkenylaryldiazoalkanes (1) to give 1H-2,3-benzodiazepines (3) takes place readily for substrates with a cis-hydrogen atom at the cyclisation site, but is blocked by phenyl or methyl groups at that position.Such

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