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[1]Benzopyrano[4,3-c]pyrazol-4(2H)-one, 3-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86100-07-4

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86100-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86100-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86100-07:
(7*8)+(6*6)+(5*1)+(4*0)+(3*0)+(2*0)+(1*7)=104
104 % 10 = 4
So 86100-07-4 is a valid CAS Registry Number.

86100-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-phenylchromeno[4,3-c]pyrazol-4-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-phenyl-2H-chromeno[4,3-c]pyrazol-4-one

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:86100-07-4 SDS

86100-07-4Downstream Products

86100-07-4Relevant academic research and scientific papers

La(OTf)3 catalyzed reaction of salicylaldehyde phenylhydrazones with β-ketoesters and activated alkynes: Facile approach for the preparation of chromenopyrazolones

Hariprasad, Kurma Siva,Prasad, Kasagani Veera,Raju, Bhimapaka China

, p. 108654 - 108661 (2016/11/30)

A facile approach has been developed for the preparation of chromenopyrazolones (5a-o, 7a-k) by the reaction of salicylaldehyde phenylhydrazones (3a-o) with β-ketoesters (4a, 4f-g) and activated alkynes (6a-e) in the presence of La(OTf)3 with good yields. However, the reaction of salicylaldehyde phenylhydrazones (3a, 3c, 3j-k, 3n) with ethyl 4-chloro-3-oxobutanoate (4e) underwent cyclization with reductive dechlorination and provided the methyl chromenopyrazolones instead of chloromethyl chromenopyrazolones. The present solvent free protocol provided the novel heterocyclic compounds.

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