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2(1H)-Isoquinolineacetic acid, 3,4-dihydro-alpha-oxo-(9CI) is a complex organic compound with a unique structure and composition. It is likely to serve as a specialized ingredient or catalyst in certain chemical reactions due to its distinctive features. However, detailed information about its physical properties, applications, and safety measures is currently unavailable, necessitating careful handling and adherence to standard laboratory safety practices.

603097-44-5

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603097-44-5 Usage

Uses

Due to the lack of specific information on the uses of 2(1H)-Isoquinolineacetic acid, 3,4-dihydro-alpha-oxo-(9CI), it is not possible to provide a detailed list of its applications. However, given its classification as an organic compound, it may potentially be used in various industries such as pharmaceuticals, chemical manufacturing, or research and development, where novel compounds are often explored for their potential applications. Further research and investigation are required to determine its exact uses and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 603097-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,0,9 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 603097-44:
(8*6)+(7*0)+(6*3)+(5*0)+(4*9)+(3*7)+(2*4)+(1*4)=135
135 % 10 = 5
So 603097-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c13-10(11(14)15)12-6-5-8-3-1-2-4-9(8)7-12/h1-4H,5-7H2,(H,14,15)

603097-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxoacetic acid

1.2 Other means of identification

Product number -
Other names 3,4-dihydroisoquinolin-2(1H)-yl(oxo)acetic 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:603097-44-5 SDS

603097-44-5Downstream Products

603097-44-5Relevant academic research and scientific papers

Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions

Huang, Hanchu,Zhang, Guojin,Chen, Yiyun

, p. 7872 - 7876 (2015)

A combination of hypervalent iodine(III) reagents (HIR) and photoredox catalysis with visible light has enabled chemoselective decarboxylative ynonylation to construct ynones, ynamides, and ynoates. This ynonylation occurs effectively under mild reaction conditions at room temperature and on substrates with various sensitive and reactive functional groups. The reaction represents the first HIR/photoredox dual catalysis to form acyl radicals from α-ketoacids, followed by an unprecedented acyl radical addition to HIR-bound alkynes. Its efficient construction of an mGlu5 receptor inhibitor under neutral aqueous conditions suggests future visible-light-induced biological applications.

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