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3-(naphthalen-1-yl)-3-oxopropanoic acid is a chemical compound with the molecular formula C13H10O3. It is a derivative of propanoic acid, featuring a naphthalene ring attached to the third carbon of the propanoic acid backbone. This organic compound is characterized by its aromatic structure and ketone functionality, which gives it unique chemical properties. It is primarily used in the synthesis of various pharmaceuticals and chemical intermediates due to its potential to form complex molecular structures. The compound's structure allows for a range of applications, including the development of drugs and other specialty chemicals, highlighting its importance in the field of organic chemistry.

76103-97-4

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76103-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76103-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76103-97:
(7*7)+(6*6)+(5*1)+(4*0)+(3*3)+(2*9)+(1*7)=124
124 % 10 = 4
So 76103-97-4 is a valid CAS Registry Number.

76103-97-4SDS

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-naphthalen-1-yl-3-oxopropanoic acid

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

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More Details:76103-97-4 SDS

76103-97-4Relevant academic research and scientific papers

Enantioselective decarboxylative Mannich reaction of β-keto acids withC-alkynylN-BocN,O-acetals: access to chiral β-keto propargylamines

Chen, Li-Jun,Li, Wei,Shen, Bao-Chun,Sun, Zhong-Wen,Xie, Hui-Ding,Zhang, Cong-Cong

, p. 8607 - 8612 (2021/10/20)

The chiral keto-substituted propargylamines are an essential class of multifunctional compounds in the field of organic and pharmaceutical synthesis and have attracted considerable attention, but the related synthetic approaches remain limited. Therefore, a concise and efficient method for the enantioselective synthesis of β-keto propargylaminesviachiral phosphoric acid-catalyzed asymmetric Mannich reaction between β-keto acids andC-alkynylN-BocN,O-acetals as easily availableC-alkynyl imine precursors has been demonstrated here, affording a broad scope of β-ketoN-Boc-propargylamines in high yields (up to 97%) with generally high enantioselectivities (up to 97?:?3 er).

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