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1H-Imidazole, 4,5-dihydro-1,5,5-trimethyl-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90265-98-8

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90265-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90265-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,6 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90265-98:
(7*9)+(6*0)+(5*2)+(4*6)+(3*5)+(2*9)+(1*8)=138
138 % 10 = 8
So 90265-98-8 is a valid CAS Registry Number.

90265-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5,5-trimethyl-4-phenyl-4H-imidazole

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,4,5-dihydro-1,5,5-trimethyl-4-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:90265-98-8 SDS

90265-98-8Downstream Products

90265-98-8Relevant academic research and scientific papers

SYNTHESIS OF 4,5-DIHYDRO-1H-IMIDAZOLES FROM 1,5-DIHYDRO-2H-IMIDAZOLES USING 'NICKEL BORIDE'

Euerby, Melvin R.,Oldroyd, Amanda C.,Waigh, Roger D.

, p. 2871 - 2877 (2007/10/02)

In situ prepared 'nickel boride' generated from sodium borohydride and nickel (II) chloride cleanly transforms 1,5-dihydro-2H-imidazoles into 4,5-dihydro-1H-imidazoles in high yields by a double bond migration.

Methylthio Activating Groups in the Synthesis of Isoquinolines

Euerby, Melvin R.,Waigh, Roger D.

, p. 127 - 128 (2007/10/02)

Methylthio activating groups have been found to improve the yields in six different isoquinoline syntheses: in four cases the improvement was from zero, in the unactivated system, to between 54 and 94percent.

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