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72142-97-3

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72142-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72142-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72142-97:
(7*7)+(6*2)+(5*1)+(4*4)+(3*2)+(2*9)+(1*7)=113
113 % 10 = 3
So 72142-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H8O3S/c1-13-12-10-8(4-5-14-10)6-7-2-3-9(16)15-11(7)12/h2-6H,1H3

72142-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-methoxyfuro[3,2-g]chromene-7-thione

1.2 Other means of identification

Product number -
Other names 8-Methoxythionepsoralen

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:72142-97-3 SDS

72142-97-3Downstream Products

72142-97-3Relevant articles and documents

Microwave-accelerated solvent-free synthesis of thioketones, thiolactones, thioamides, thionoesters, and thioflavonoids

Varma, Rajender S.,Kumar, Dalip

, p. 697 - 700 (2008/02/11)

Formula presented An expeditious, solvent-free, and high yield conversion of ketones, flavones, isoflavones, lactones, amides, and esters to the corresponding thio analogues is described utilizing Lawesson's reagent in a process that circumvents the use of dry solvents and excess of the reagent.

PHOTOBIOLOGICAL PROPERTIES OF FUROTHIOCOUMARINS IN SACCHAROMYCES CEREVISIAE

Juettermann, R.,Averbeck, D.,Averbeck, S.,Bastian, G.,Royer, R.

, p. 3 - 13 (2007/10/02)

Nine furothiocoumarins corresponding to psoralen, 8-methylpsoralen, 3-carbethoxy-8-methylpsoralen, 8-methoxysporalen, pseudosporalen, angelicin, isopseudosporalen, allopsoralen and pseudoisosporalen were synthesized by treating furocoumarins with phosphorus pentasulfide. Photobiological studies on haploid yeast cells (Saccharomyces cerevisiae) revealed that the furocoumarins exert some photoactivity on cell survival and the induction of mitochondrial damage.In most cases, the furothiocoumarins were less active than their furocoumarinic counterparts and exhibited a preference for a monofunctional type of action.A certain photochemotherapeutic activity can be suggested.

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