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4H-1-Benzopyran-4-thione, 3-hydroxy-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85726-15-4

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85726-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85726-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,2 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85726-15:
(7*8)+(6*5)+(5*7)+(4*2)+(3*6)+(2*1)+(1*5)=154
154 % 10 = 4
So 85726-15-4 is a valid CAS Registry Number.

85726-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-phenylchromene-4-thione

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-thione,3-hydroxy-2-phenyl

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:85726-15-4 SDS

85726-15-4Upstream product

85726-15-4Relevant academic research and scientific papers

Photophysical properties of hydroxy-substituted flavothiones

Elisei, Fausto,Lima, Joao C.,Ortica, Fausto,Aloisi, Gian G.,Costa, Manuela,Leitao, Emilia,Abreu, Isabel,Dias, Antonio,Bonifacio, Vasco,Medeiros, Jorge,Macanita, Antonio L.,Becker, Ralph S.

, p. 6095 - 6102 (2000)

Flavothione and a number of synthesized hydroxy- (mono- and di-) substituted flavothiones have been thoroughly examined, particularly regarding their absorption, emission, photophysical (triplet yields and lifetimes), and oxygen-photosensitizing characteristics. These were all studied as a function of the nature of the solvent (four), which was particularly critical in terms of aiding in determining the energy and configurational nature of the lowest triplet state as well as the mechanism of intersystem crossing. Theoretical calculations were also performed. Both the location and number of hydroxyl groups have a substantial impact on the nature of the lowest excited triplet state as well as on the relative location of the two lowest excited singlet and triplet states. These in turn affect the magnitude and even the existence of triplet-state occupation as well as the ability to sensitize oxygen (to singlet oxygen). Three groups of compounds exist as characterized by the configurational nature of the triplet and the mechanism of intersystem crossing, or the essential absence of intersystem crossing altogether. The quantum yield of singlet oxygen formation is high for one group where the T(π, π*) state is lowest and generally high in another group where the T(n, π*) state is lowest, except in ethanol where competitive H-atom abstraction occurs. The potential of all hydroxy compounds as photosensitizers is evaluated.

CO Targeted delivery system and construction method and application thereof

-

Paragraph 0055-0057; 0069; 0078; 0085; 0092; 0099; 0106; ..., (2021/10/30)

The invention discloses CO targeted delivery system and a construction method and application thereof, and belongs to the technical field of nano material CO targeted delivery. The nano particle comprises a carbon monoxide prodrug and an oxalate or a poly

Flavothionato metal complexes: Implications for the use of hydroxyflavothiones as green pesticides

Tran, Ba L.,Cohen, Seth M.

, p. 203 - 205 (2008/02/07)

Transition-metal complexes of 3-hydroxyflavothiones have been prepared and structurally characterized; the photochemical properties of these complexes have been examined and are discussed in the context of the use of these compounds as photodegradable pes

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