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37570-85-7

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37570-85-7 Usage

Structure

Contains a five-membered ring with two nitrogen atoms at positions 1 and 3
The ring structure is characteristic of imidazoles

Substitution

Methyl group at the 1-position
A side chain attached to the imidazole ring

Class

Organic compounds
Consists of elements such as carbon, hydrogen, and nitrogen

Potential applications

Pharmaceutical, agrochemical, and materials science
Can be used in the development of drugs, pesticides, and other materials

Biological activity

May exhibit biological activity
Can interact with biological systems and potentially produce effects

Synthesis

Can be used as a building block in the synthesis of other compounds
Can be combined with other chemical groups to create new molecules

Safety

Handle with care and follow safety protocols
Due to potential hazards and reactivity, it is important to take precautions when working with this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 37570-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,7 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37570-85:
(7*3)+(6*7)+(5*5)+(4*7)+(3*0)+(2*8)+(1*5)=137
137 % 10 = 7
So 37570-85-7 is a valid CAS Registry Number.

37570-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-imidazol-2-yl)-1-methylimidazole

1.2 Other means of identification

Product number -
Other names 2,2'-Bi-1H-imidazole,1-methyl

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:37570-85-7 SDS

37570-85-7Downstream Products

37570-85-7Relevant articles and documents

Long tethers binding redox centers to polymer backbones enhance electron transport in enzyme "wiring" hydrogels

Mao, Fei,Mano, Nicolas,Heller, Adam

, p. 4951 - 4957 (2003)

A redox hydrogel with an apparent electron diffusion coefficient (Dapp) of (5.8 ± 0.5) × 10-6 cm2 s-1 is described. The order of magnitude increase in Dapp relative to previously studied redox hydrogels results from the tethering of redox centers to the backbone of the cross-linked redox polymer backbone through 13 atom spacer arms. The long and flexible tethers allow the redox centers to sweep electrons from large-volume elements and to collect electrons of glucose oxidase efficiently. The spacer arms make the collection of electrons from glucose oxidase so efficient that glucose is electrooxidized already at -0.36 V versus Ag/AgCl, the reversible potential of the redox potential of the FAD/FADH2 centers of the enzyme at pH 7.2. The limiting current density of 1.15 mA cm-2 is reached at a potential as low as -0.1 V versus Ag/AgCl. The novel redox center of the polymer is a tris-dialkylated N,N′-biimidazole Os2+/3+ complex. Its redox potential, -0.195 V versus Ag/AgCl, is 0.8 V reducing relative to that of Os(bpy)2+/3+, its 2,2′-bipyridine analogue.

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