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Pyrazolo[1,5-a]pyrimidin-7(4H)-one, 3,3'-dithiobis[4-ethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86969-28-0

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86969-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86969-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,6 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86969-28:
(7*8)+(6*6)+(5*9)+(4*6)+(3*9)+(2*2)+(1*8)=200
200 % 10 = 0
So 86969-28-0 is a valid CAS Registry Number.

86969-28-0SDS

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 4-ethyl-3-[(4-ethyl-7-oxo-2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)disulfanyl]-2-phenylpyrazolo[1,5-a]pyrimidin-7-one

1.2 Other means of identification

Product number -
Other names Pyrazolo[1,5-a]pyrimidin-7(4H)-one,3,3'-dithiobis[4-ethyl-2-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:86969-28-0 SDS

86969-28-0Downstream Products

86969-28-0Relevant articles and documents

2-Phenylpyrazolo[1,5-a]pyrimidin-7-ones. A new class of nonsteroidal antiinflammatory drugs devoid of ulcerogenic activity

Auzzi, Gabriella,Bruni, Fabrizio,Cecchi, Lucia,Costanzo, Annarella,Vettori, Lorenzo Pecori,et al.

, p. 1706 - 1709 (2007/10/02)

Syntheses of some pyrazolo[1,5-a]pyrimidines were performed in order to study the relationship between structural modifications on the parent 4,7-dihydro-2-phenylpyrazolo[1,5-a]pyrimidin-7-one (1) and their antiinflammatory properties. The modifications c

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