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2-Propenoic acid, 2-(acetylamino)-3-[4-(acetyloxy)-3-methoxyphenyl]-, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55739-56-5

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55739-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55739-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,3 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55739-56:
(7*5)+(6*5)+(5*7)+(4*3)+(3*9)+(2*5)+(1*6)=155
155 % 10 = 5
So 55739-56-5 is a valid CAS Registry Number.

55739-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-α-acetamido-4-acetoxy-3-methoxy-cinnamic acid

1.2 Other means of identification

Product number -
Other names (Z)-α-Acetamido-4-acetoxy-3-methoxycinnamic 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:55739-56-5 SDS

55739-56-5Relevant academic research and scientific papers

A modified synthesis of (±)-β-aryllactic acids

Wong,Xu,Chang,Lee

, p. 793 - 797 (2007/10/02)

The synthesis of racemic forms of the reportedly active principle of Danshen, namely (±)-β-(3,4-dihydroxyphenyl)lactic acid [(±)3-(3,4-dihydroxyphenyl)-2-hydroxypropanoic acid] and its seven racemic derivatives is reported.

Asymmetric Catalyses. V. Enantioselective Amino Acid Synthesis by Hydrogenation of Prochiral Olefins with Rh-Complexes of the New Optically Active Chelating Phosphane Norphos

Brunner, Henri,Pieronczyk, Willigis,Schoenhammer, Beate,Streng, Karin,Bernal, Ivan,Korp, Jim

, p. 1137 - 1149 (2007/10/02)

Racemic bicyclohept-5-ene-2,3-diylbis(diphenylphosphane oxide), NorphosO, can be resolved with (-)-di-O-benzoyltartaric acid, (-)-DBW.The X-ray structure analysis of the diastereomer (-)-NorphosO/(-)-DBW, which is less soluble in ethanol, exhibits strong hydrogen bonds between the carboxylic groups of DBW and the PO groups.The bonding of the DBW-carboxylic groups to different NorphosO units leads to the formation of infinite close-packed chains.From the internal comparison with (-)-DBW the absolute configuration follows as (2R,3R) for (-)-Norphos.The chelating phosphanes (+)- and (-)-Norphos, obtained by SiHCl3-reduction of (+)- and (-)-NorphosO, respectively, afford neutral and cationic Rh-complexes which, with H2 at room temperature and atmospheric pressure within a few hours, give quantitative hydrogenation of α-(acetylamino)cinnamic acid, α-(acetylamino)acrylic acid and Dopa precursors.The optical yields vary between 79 and 97percent.

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