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α-Methyl-9-oxo-9H-xanthene-2-acetic acid is a chemical compound with the molecular formula C14H10O4. It is a derivative of xanthene, a tricyclic aromatic compound, and features a methyl group at the alpha position, an oxo group at the 9 position, and an acetic acid group at the 2 position. α-Methyl-9-oxo-9H-xanthene-2-acetic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. Its structure provides a foundation for further chemical modifications, making it a valuable component in the development of new molecules with specific therapeutic or pesticidal properties.

30087-33-3

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30087-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30087-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,8 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30087-33:
(7*3)+(6*0)+(5*0)+(4*8)+(3*7)+(2*3)+(1*3)=83
83 % 10 = 3
So 30087-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O4/c1-9(16(18)19)10-6-7-14-12(8-10)15(17)11-4-2-3-5-13(11)20-14/h2-9H,1H3,(H,18,19)

30087-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(9-Oxo-9H-xanthen-2-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names (Methylthio)acetic Acid Ethyl Ester

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:30087-33-3 SDS

30087-33-3Downstream Products

30087-33-3Relevant academic research and scientific papers

Development of photo-controllable hydrogen sulfide donor applicable in live cells

Fukushima, Naoki,Ieda, Naoya,Kawaguchi, Mitsuyasu,Sasakura, Kiyoshi,Nagano, Tetsuo,Hanaoka, Kenjiro,Miyata, Naoki,Nakagawa, Hidehiko

, p. 175 - 178 (2015)

Hydrogen sulfide (H2S) has multiple physiological roles, for example, in vasodilation and inflammation. It is a highly reactive gas under ambient conditions, so controllable H2S donors are required for studying its biological functions. Here, we describe the design, synthesis and application of a H2S donor (SPD-2) that utilizes xanthone photochemistry to control H2S release. H2S generation from SPD-2 was completely dependent on UVA-irradiation (325-385 nm), as confirmed by methylene blue assay and by the use of a H2S-selective fluorescent probe. SPD-2 was confirmed to provide controlled H2S delivery in live cells, and should be suitable for various biological applications.

Photolabile protecting groups based on the singlet state photodecarboxylation of xanthone acetic acid

Blake, Jessie A.,Lukeman, Matthew,Scaiano, Juan C.

supporting information; experimental part, p. 4127 - 4135 (2009/09/04)

A new photolabile protecting group (PPG) for carboxylic acids and amineshas been developed based on the rapid singlet state photodecarboxylatio n of xanthone acetic acids with several features that are superior to many other systems. We demonstrate that t

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