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162012-30-8

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162012-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162012-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 162012-30:
(8*1)+(7*6)+(6*2)+(5*0)+(4*1)+(3*2)+(2*3)+(1*0)=78
78 % 10 = 8
So 162012-30-8 is a valid CAS Registry Number.

162012-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methylsulfanylphenyl)-4-phenyl-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 2(5H)-Furanone,4-[4-(methylthio)phenyl]-3-phenyl

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:162012-30-8 SDS

162012-30-8Relevant articles and documents

PURIFIED FORMS OF ROFECOXIB, METHODS OF MANUFACTURE AND USE

-

, (2020/06/10)

The subject matter disclosed herein relates to rofecoxib, also known as TRM-201 or RXB-201, its method of manufacture, and use. In certain aspects, the highly pure or substantially pure rofecoxib as provided herein has a favorable purity profile and is the active ingredient in a pharmaceutical composition that is administered to treat or prevent a number of conditions, including pain associated with a condition caused by a bleeding disorder.

Racemic and chiral sulfoxides as potential prodrugs of the COX-2 inhibitors Vioxx and Arcoxia

Caturla, Francisco,Amat, Merce,Reinoso, Raquel F.,Cordoba, Monica,Warrellow, Graham

, p. 3209 - 3212 (2007/10/03)

The preparation of the sulfoxide analogues 2 and 4, and their enantiomeric pure forms is discussed as well as their potential to act as prodrugs to the potent and selective sulfone-containing COX-2 inhibitors rofecoxib and etoricoxib. Sulfoxides 2 and 4 w

Preparation of aryl-substituted butenolides using mucohalic acids

-

Page/Page column 8-9, (2008/06/13)

Methods and materials for preparing 3-aryl-2-buten-4-olides and 2,3-bisaryl-2-buten-4-olides are disclosed. The methods include reacting a mucohalic acid with a reducing agent to give a 2,3-dihalo-2-buten-4-olide, which undergoes at least one Pd catalyzed cross-coupling reaction with an arylboronic acid.

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