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2,5-dichloro-4-nitro-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15965-32-9

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15965-32-9 Usage

Physical state

Yellow crystalline solid
Antimicrobial properties
Toxic and potentially harmful

Specific content

Used in various industrial and pharmaceutical applications
Active ingredient in antifungal and antibacterial medications
Used in the synthesis of other organic compounds
Reagent in chemical reactions

Check Digit Verification of cas no

The CAS Registry Mumber 15965-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15965-32:
(7*1)+(6*5)+(5*9)+(4*6)+(3*5)+(2*3)+(1*2)=129
129 % 10 = 9
So 15965-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C3HCl2N3O2/c4-1-2(8(9)10)7-3(5)6-1/h(H,6,7)

15965-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dichloro-4-nitro-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-5-nitro-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:15965-32-9 SDS

15965-32-9Downstream Products

15965-32-9Relevant academic research and scientific papers

METHOD FOR PRODUCING 4-NITROIMIDAZOLE COMPOUND

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Page/Page column 73-74, (2008/06/13)

The present invention provides a method for producing a 4-nitroimidazole compound represented by general formula (1) at high yield and at high purity by a safe method causing few dangers such as explosion. The production method of the present invention comprises iodinating a 4-nitroimidazole compound represented by general formula (2): wherein each of X1 and X2 represents a chlorine atom or bromine atom, and then reducing the obtained 5-iodo-4-nitroimidazole compound represented by general formula (3): wherein X2 is the same as defined above.

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