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3528-23-2

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3528-23-2 Usage

Structure

Contains a benzene ring fused to a pyrone ring

Natural Sources

Found in tonka beans, cinnamon, sweet clover, and other plant species

Applications

Used in the production of perfumes and flavorings due to its pleasant, sweet scent
Acts as a precursor to the drug warfarin in medicine, owing to its anticoagulant properties

Regulation

Its use in food and beverages is regulated in several countries due to potential liver damage associated with excessive consumption

Versatility

Widely used in fragrance, flavor, and medicine industries

Check Digit Verification of cas no

The CAS Registry Mumber 3528-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3528-23:
(6*3)+(5*5)+(4*2)+(3*8)+(2*2)+(1*3)=82
82 % 10 = 2
So 3528-23-2 is a valid CAS Registry Number.

3528-23-2SDS

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 4-oxo-4H-naphtho[1,2-b]pyran

1.2 Other means of identification

Product number -
Other names naphtho[1,2-b]pyan-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:3528-23-2 SDS

3528-23-2Relevant articles and documents

Synthesis and antibacterial studies of 6-aryl-2,2a-dihydro-naphtho- [2′,1′-5,6]pyrano[4,3-e][1,2,4]triazolo[3,4-b][1,3,4]thiadiazine and its derivatives

Karnik,Malviya,Kulkarni,Jaimini,Jadhav

, p. 489 - 493 (2006)

Chemoselective synthesis of novel hetero cyclopenta[b]chrysene derivatives, namely, 6-Aryl-2,2a-dihydro-naphtho[2′,1′,5,6]pyrao[4,3-e][1,2,4] triazolo[3,4-b][1,3,4]thiadiazine (4a-j) under neutral condition has been described. These molecules exhibited go

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