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103986-39-6

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103986-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103986-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,8 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103986-39:
(8*1)+(7*0)+(6*3)+(5*9)+(4*8)+(3*6)+(2*3)+(1*9)=136
136 % 10 = 6
So 103986-39-6 is a valid CAS Registry Number.

103986-39-6SDS

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 5,7-dihydroxy-3,4-dimethylchromen-2-one

1.2 Other means of identification

Product number -
Other names 5,7-dihydroxy-3,4-dimethyl-coumarin

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:103986-39-6 SDS

103986-39-6Downstream Products

103986-39-6Relevant articles and documents

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John,Israelstam

, p. 240 (1961)

-

Introduction of poly(4-vinylpyridinium) perchlorate as a new, efficient, and versatile solid acid catalyst for one-pot synthesis of substituted coumarins under ultrasonic irradiation

Khaligh, Nader Ghaffari,Shirini, Farhad

, p. 26 - 31,6 (2013)

Poly(4-vinylpyridinium) perchlorate, is a supported, recyclable, eco-benign catalyst for synthesis of substituted coumarins via Pechmann reaction using ultrasound irradiation at room temperature and neat condition in high yields with short reaction times. The catalyst was studied by FT-IR, X-ray diffraction, scanning electron microscope, thermo-gravimetric and energy dispersion X-ray analyses. All the products were extensively characterized by 1H NMR, FT-IR, MS and melting point analyses. This methodology offers momentous improvements over various options for the synthesis of coumarins with regard to yield of products, simplicity in operation and green aspects by avoiding toxic catalysts and solvents. Further, the catalyst can be reused and recovered for several times without loss of activity.

A solvent-free synthesis of coumarins using a Wells-Dawson heteropolyacid as catalyst

Romanelli,Bennardi,Ruiz,Baronetti,Thomas,Autino

, p. 8935 - 8939 (2004)

Seventeen examples are resolved, most of them in good to excellent yields, using the cheap WD catalyst. Substituted coumarins are synthesized from phenols and β-ketoesters by the Pechmann reaction, using a Wells-Dawson heteropolyacid (H6P2W18O62? 24H2O) as catalyst by a solvent-free procedure. This one requires low reaction times, 130°C temperature and as little as 1 mol % of Wells-Dawson acid, obtaining good to excellent yields of coumarins. The catalyst showed to be reusable with no differences in the yields. The results are compared with those of the reactions performed in toluene solution. The presented synthetic procedure is a convenient, clean and fast alternative for synthesizing 4-substituted coumarins (17 examples).

Synthesis of coumarins catalyzed by eco-friendly W/ZrO2 solid acid catalyst

Reddy,Reddy,Giridhar

, p. 3603 - 3607 (2001)

Synthesis of substituted coumarins via reactions of resorcinol and substituted resorcinol with ethyl acetoacetate and ethyl α-methylacetoacetate (Pechmann reaction) are reported, in which the production of environmentally harmful waste streams is minimized by the use of a novel solid acid catalyst.

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