Welcome to LookChem.com Sign In|Join Free
  • or
5-Benzofurancarboxaldehyde, 6-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20073-22-7

Post Buying Request

20073-22-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

20073-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20073-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20073-22:
(7*2)+(6*0)+(5*0)+(4*7)+(3*3)+(2*2)+(1*2)=57
57 % 10 = 7
So 20073-22-7 is a valid CAS Registry Number.

20073-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-1-benzofuran-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-benzofurancarbaldehyde,6-hydroxy

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:20073-22-7 SDS

20073-22-7Relevant academic research and scientific papers

Condensation of salicylaldehydes with ethyl 4,4,4-trichloro-3-oxobutanoate: A facile approach for the synthesis of substituted 2H-chromene-3-carboxylates

Sairam, Mudulkar,Saidachary, Gannerla,Raju, Bhimapaka China

supporting information, p. 1338 - 1343 (2015/03/04)

A highly efficient and simple protocol has been developed for the preparation of ethyl 2-oxo-2H-chromene-3-carboxylates 3a-v by the condensation of salicylaldehydes 1a-v with ethyl 4,4,4-trichloro-3-oxobutanoate 2 for the first time. The reaction is proceeding via Knoevenagel pathway followed by a selective addition of the phenolic hydroxyl group to the carbonyl group adjacent to the CCl3 group rather than ester carbonyl due to a strong electron withdrawing effect and produced coumarin derivative 3a with the elimination of CHCl3.

A NEW PHOTOPRODUCT FROM FUROCOUMARIN PHOTOLYSIS IN DILUTE AQUEOUS SOLUTION: 5-FORMYL-6-HYDROXYBENZOFURAN

Marley, Karen A.,Larson, Richard A.

, p. 503 - 505 (2007/10/02)

This paper presents the analysis and identification of an unstable product previously undescribed from furocoumarin photolysis, 5-formyl-6-hydroxybenzofuran. Reverse-phase chromatography and solid-phase extraction techniques allowed its isolation.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 20073-22-7