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62935-72-2

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62935-72-2 Usage

Uses

Different sources of media describe the Uses of 62935-72-2 differently. You can refer to the following data:
1. A precursor to coumarin-type fluorescent reagents
2. Key intermidiate for the synthesis of fluorescence probes in chromatographic detection. Shows local anesthetic activity.
3. 7-Methoxycoumarin-4-acetic acid is a precursor to coumarin-type fluorescent reagents. It has been uses as fluorescent probe in preparation of two novel LysB29 selectively labeled fluorescent derivatives of human insulin, in the preparation of cell-penetrating peptide transportan 10 (tp10) and as fluorescent label for peptides.

Check Digit Verification of cas no

The CAS Registry Mumber 62935-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62935-72:
(7*6)+(6*2)+(5*9)+(4*3)+(3*5)+(2*7)+(1*2)=142
142 % 10 = 2
So 62935-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O5/c1-16-8-2-3-9-7(4-11(13)14)5-12(15)17-10(9)6-8/h2-3,5-6H,4H2,1H3,(H,13,14)

62935-72-2 Well-known Company Product Price

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  • Aldrich

  • (235199)  7-Methoxycoumarin-4-aceticacid  97%

  • 62935-72-2

  • 235199-500MG

  • 1,478.88CNY

  • Detail
  • Aldrich

  • (235199)  7-Methoxycoumarin-4-aceticacid  97%

  • 62935-72-2

  • 235199-1G

  • 2,552.94CNY

  • Detail

62935-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-methoxy-2-oxochromen-4-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (7-methoxy-2-oxo-2H-chromen-4-yl)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:62935-72-2 SDS

62935-72-2Relevant articles and documents

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Laskowski,Clinton

, p. 3987,3989 (1950)

-

Synthesis of 2-(2-oxo-2H-chromen-4-yl)acetamides as potent acetylcholinesterase inhibitors and molecular insights into binding interactions

Kara, Jiraporn,Suwanhom, Paptawan,Wattanapiromsakul, Chatchai,Nualnoi, Teerapat,Puripattanavong, Jindaporn,Khongkow, Pasarat,Lee, Vannajan Sanghiran,Gaurav, Anand,Lomlim, Luelak

, (2019/07/08)

Sixteen novel coumarin-based compounds are reported as potent acetylcholinesterase (AChE) inhibitors. The most active compound in this series, 5a (IC50 0.04 ± 0.01 μM), noncompetitively inhibited AChE with a higher potency than tacrine and gala

Synthetic and Structural Studies on Novel 4,3′-Bicoumarins

Pujar, Kiran K.,Kulkarni, Manohar V.,Alawandi, Ganesh N.,Anilkumar,Basanagouda, Mahantesha

, p. 2043 - 2052 (2015/08/18)

A series of directly linked 4-3′ bicoumarins have been synthesized by both Knoevenagel and Perkin reactions. This single-step transformation was accomplished by the reaction of coumarin-4-acetates with substituted salicylaldehydes in presence of piperidin

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