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70711-53-4

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  • BES-Na/2-[N,N-Bis(2-hydroxyethyl)amino]ethanesulfonic acid sodium salt(66992-27-6)

    Cas No: 70711-53-4

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70711-53-4 Usage

Uses

Phenindione-D5 is a proton pump inhibitor and traditional nonsteroidal anti-inflammatory drug used for acute interstitial nephritis and acute kidney injury.;Labeled Phenindione-D5, intended for use as an internal standard for the quantification

Check Digit Verification of cas no

The CAS Registry Mumber 70711-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,1 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70711-53:
(7*7)+(6*0)+(5*7)+(4*1)+(3*1)+(2*5)+(1*3)=104
104 % 10 = 4
So 70711-53-4 is a valid CAS Registry Number.

70711-53-4SDS

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 2-pentadeuteriophenyl-indan-1,3-dione

1.2 Other means of identification

Product number -
Other names Phenindione-d5

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:70711-53-4 SDS

70711-53-4Downstream Products

70711-53-4Relevant articles and documents

Ru(II)-Catalyzed C-H Activation and Alkyne Annulation Reaction of Phenyl Indandiones: Synthesis of Spirobi[indene]diones

Bora, Bidisha R.,Sultana, Sabera,Sarma, Bipul,Gogoi, Sanjib

, p. 2907 - 2915 (2022/04/25)

A Ru(II)-catalyzed synthesis of spirobi[indene]dione from phenyl indandione and alkyne is reported. This metal-catalyzed cyclization reaction proceeds through hydroxy group directed C(sp2)-H bond activation, keto-enol tautomerization and alkyne annulation pathways.

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