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6-PHENYL-PYRAZINECARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90701-04-5

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90701-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90701-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,0 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90701-04:
(7*9)+(6*0)+(5*7)+(4*0)+(3*1)+(2*0)+(1*4)=105
105 % 10 = 5
So 90701-04-5 is a valid CAS Registry Number.

90701-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-phenylpyrazine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-PHENYL-PYRAZINECARBONITRILE

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:90701-04-5 SDS

90701-04-5Downstream Products

90701-04-5Relevant academic research and scientific papers

Synthesis and Herbicidial Activity of 6-Phenyl-5-Propylamino-2-Pyrazinecarbonitriles and Related Compounds

Nakamura, Akira,Ono, Matsuo,Segawa, Hirozo,Takematsu, Tetsuo

, p. 1009 - 1016 (2007/10/02)

6-Phenyl- and 5-phenyl-2-pyrazinecarbonitriles with or without a propylamino group at the 3-, 5- or 6-position of the pyrazine ring were prepared together with some related compounds from the corresponding 2,3-pyrazinedicarbonitriles.Their hebicidial activities against barnyardgrass and broadleaf weeds were examined in pot tests.The 6-phenyl-2-pyrazinecarbonitriles were relatively potent compared with the 5-phenyl derivatives.Moreover, the presence of a propylamino group at the 5-position of the 6-phenyl-2-pyrazinecarbonitriles was closely related to an increase in activity.

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