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2(3H)-Furanone,4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylene)dihydro-,(3Z,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22554-63-8

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22554-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22554-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22554-63:
(7*2)+(6*2)+(5*5)+(4*5)+(3*4)+(2*6)+(1*3)=98
98 % 10 = 8
So 22554-63-8 is a valid CAS Registry Number.

22554-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-isohibalactone

1.2 Other means of identification

Product number -
Other names (-)-hibalactone

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:22554-63-8 SDS

22554-63-8Upstream product

22554-63-8Downstream Products

22554-63-8Relevant academic research and scientific papers

Chiral Synthesis of Lignan Lactones, (-)-Hinokinin, (-)-Deoxypodorhizone, (-)-Isohibalactone and (-)-Savinin by Means of Enantioselective Deprotonation

Honda, Toshio,Kimura, Nobuaki,Sato, Shigeki,Kato, Daishiro,Tominaga, Hideo

, p. 1043 - 1046 (2007/10/02)

Chiral synthesis of lignan lactones, (-)-hinokinin, (-)-deoxypodorhizone, (-)-isohibalactone and (-)-savinin, has been achieved by employing an enantioselective deprotonation of 3-(3,4-methylenedioxybenzyl)cyclobutanone with lithium (S,S')-α,α'-dimethylbenzylamide, as a key step.

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