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83688-40-8

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83688-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83688-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83688-40:
(7*8)+(6*3)+(5*6)+(4*8)+(3*8)+(2*4)+(1*0)=168
168 % 10 = 8
So 83688-40-8 is a valid CAS Registry Number.

83688-40-8SDS

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 7,9-dihydroxy-2,3-dihydro-1H-cyclopenta[c]chromen-4-one

1.2 Other means of identification

Product number -
Other names 3,4-cyclopentyl-5,7-dihydroxycoumarin

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:83688-40-8 SDS

83688-40-8Downstream Products

83688-40-8Relevant articles and documents

Nano-BFn/cellulose: a bio-based nano-catalyst for synthesis of bio-active 7-hydroxycoumarins

Mirjalili, Bi Bi Fatemeh,Bamoniri, Abdolhamid,Fazeli-Attar, Seyede Azita

, p. 839 - 851 (2022/01/20)

Nano-BFn/cellulose as a modified bio-based nano-catalyst has been synthesized from nanocellulose and boron triflouride via very simple steps. This novel nano-catalyst exhibited many advantages in the synthesis of 7-hydroxycoumarins such as good

TETRIACYCLODIPYRANYL COUMARINS AND THE ANTI-HIV AND ANTI-TUBERCULOSIS USES THEREOF

-

Page/Page column 48, (2010/08/18)

The present invention relates to tctracyclodipyrano-coumarin compounds of general formula (I), wherein the substituents are defined herein. These compounds exihibit dual biological activities of anti human immunodeficiency virus type 1 (HIV-1) infection a

Microwave initiated reactions: Pechmann coumarin synthesis, Biginelli reaction, and acylation

Manhas, Maghar S.,Ganguly, Subhendu N.,Mukherjee, Somdatta,Jain, Amit K.,Bose, Ajay K.

, p. 2423 - 2425 (2007/10/03)

An energy-efficient protocol has been developed for solvent-free reactions that are mildly exothermic but not spontaneous. The exothermic reaction mixture-on several g-scale-is exposed for about 30 s to low power (about 200 W) microwaves and then the microwave oven is switched off. After this short burst of energy, the exothermic reaction gets initiated and proceeds on its own to completion. A number of coumarins were synthesized by the Pechmann reaction using this strategy.

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