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66548-88-7

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66548-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66548-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66548-88:
(7*6)+(6*6)+(5*5)+(4*4)+(3*8)+(2*8)+(1*8)=167
167 % 10 = 7
So 66548-88-7 is a valid CAS Registry Number.

66548-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-6-[4-(trifluoromethyl)phenyl]pyridazine

1.2 Other means of identification

Product number -
Other names Pyridazine,3-chloro-6-[4-(trifluoromethyl)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:66548-88-7 SDS

66548-88-7Relevant articles and documents

Pd-catalyzed chemoselective cross-coupling reaction of triaryl- or triheteroarylbismuth compounds with 3,6-dihalopyridazines

Urgin, Karene,Aube, Christophe,Pipelier, Muriel,Blot, Virginie,Thobie-Gautier, Christine,Sengmany, Stephane,Lebreton, Jacques,Leonel, Eric,Dubreuil, Didier,Condon, Sylvie

supporting information, p. 117 - 124 (2013/02/22)

The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. Copyright

6-Phenyl-1,2,4-triazolo[4,3-b]pyridazine hypotensive agents

-

, (2008/06/13)

This disclosure describes novel substituted 6-phenyl-1,2,4-triazolo[4,3-b]pyridazines useful as hypotensive agents.

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