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Cyclohexanol, 1-(1-methyl-1H-imidazol-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91010-59-2

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91010-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91010-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,1 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91010-59:
(7*9)+(6*1)+(5*0)+(4*1)+(3*0)+(2*5)+(1*9)=92
92 % 10 = 2
So 91010-59-2 is a valid CAS Registry Number.

91010-59-2SDS

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 1-(1-methylimidazol-2-yl)cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names Cyclohexanol,1-(1-methyl-1H-imidazol-2-yl)

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:91010-59-2 SDS

91010-59-2Relevant academic research and scientific papers

Facile Syntheses of 2-Ethenyl-1H-imidazoles

Ohta, Shunsaku,Matsukawa, Masami,Ohashi, Norihiko,Nagayama, Kayo

, p. 78 - 81 (1990)

2-Ethenyl-1H-imidazoles 6 were readily prepared by treating 2-(1-hydroxyalkyl)-1H-imidazoles 5 with hot acetic anhydride.Several convenient procedures to precursors of 6 are described.

Isoprene-catalyzed lithiation of imidazole: Synthesis of 2-(hydroxyalkyl)- and 2-(aminoalkyl)imidazoles

Torregrosa, Rosario,Pastor, Isidro M.,Yus, Miguel

, p. 11148 - 11155 (2007/10/03)

2-Lithioimidazole was prepared by means of a new protocol, which consists of a slight excess of lithium metal in the presence of a substoichiometric amount of isoprene (20 mol%) in THF at room temperature. By reacting this organolithium with carbonyl elec

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