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2-Nitro-4-(1-pyrrolidinylmethyl)-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68406-49-5

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68406-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68406-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68406-49:
(7*6)+(6*8)+(5*4)+(4*0)+(3*6)+(2*4)+(1*9)=145
145 % 10 = 5
So 68406-49-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N4O2/c13-12(14)8-9-5-7(10-8)6-11-3-1-2-4-11/h5H,1-4,6H2,(H,9,10)

68406-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-5-(pyrrolidin-1-ylmethyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-nitro-4-pyrrolidin-1-ylmethyl-1H-imidazole

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:68406-49-5 SDS

68406-49-5Downstream Products

68406-49-5Relevant academic research and scientific papers

DERIVATIVES OF QUINOLINES AND QUINOXALINES AS PROTEIN TYROSINE KINASE INHIBITORS

-

Page/Page column 77, (2009/12/27)

The invention relates to compounds of Formula (I), wherein the substituens are as defined in the specification, in free form or in the form of a pharmaceutically acceptable salt, solvate, ester, N-oxide thereof; processes for the preparation thereof; to p

Nitroimidazoles: Part XVIII- Mannich Reactions of Azomycin-2-nitro-4,5-bisaminoalkylimidazoles

Parthasarathy, P. C.,Desai, H. K.,Saindane, M. T.

, p. 157 (2007/10/02)

Mannich reaction of azomycin (1) (2-nitroimidazole) gives 4-monoaminoalkyl (2) or 4,5-bisaminoalkyl derivatives (4a and 4c) in preference to N-substituted compounds.Methylation of 4a affords the 1-methyl derivative (4b).The structures of these products are based on spectroscopic evidences.

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