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ALFA-METHYL-5H-[1] BENZOPYRANO [2,3-B] PYRIDINE-7-ACETIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86618-09-9

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86618-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86618-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,1 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86618-09:
(7*8)+(6*6)+(5*6)+(4*1)+(3*8)+(2*0)+(1*9)=159
159 % 10 = 9
So 86618-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO3/c1-3-20-17(19)11(2)12-6-7-15-14(9-12)10-13-5-4-8-18-16(13)21-15/h4-9,11H,3,10H2,1-2H3

86618-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(5H-chromeno[2,3-b]pyridin-7-yl)propanoate

1.2 Other means of identification

Product number -
Other names alfa-Methyl-5H-[1] benzopyrano [2,3-b] pyridine-7-acetic acid ethyl ester

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:86618-09-9 SDS

86618-09-9Downstream Products

86618-09-9Relevant academic research and scientific papers

Formation and Disproportionation of Xanthenols to Xanthenes and Xanthones and Their Use in Synthesis

Shi, Zeyu,Chen, Si,Xiao, Qiong,Yin, Dali

, p. 3334 - 3343 (2021/02/05)

A facile and versatile strategy employing TiCl4-mediated cyclization followed by a Cannizzaro reaction has been developed for the synthesis of various xanthene derivatives. The reaction proceeded smoothly to afford both xanthenes/xanthones or their sulfur derivatives and tolerated a wide range of electronically diverse substrates. Using this methodology, pranoprofen was synthesized in three steps in 59% overall yield from commercially available starting materials.

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