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Benzene, 2-chloro-1,3,4,5-tetranitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10420-84-5

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10420-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10420-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10420-84:
(7*1)+(6*0)+(5*4)+(4*2)+(3*0)+(2*8)+(1*4)=55
55 % 10 = 5
So 10420-84-5 is a valid CAS Registry Number.

10420-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,6-tetranitrochlorobenzene

1.2 Other means of identification

Product number -
Other names 2.3.4.6-Tetranitro-chlorbenzol

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:10420-84-5 SDS

10420-84-5Upstream product

10420-84-5Downstream Products

10420-84-5Relevant academic research and scientific papers

Nitrocarbons. 4. Reaction of Polynitrobenzenes with Hydrogen Halides. Formation of Polynitrohalobenzenes

Nielsen, Arnold T.,Chafin, Andrew P.,Christian, Stephen L.

, p. 4575 - 4580 (2007/10/02)

Hexanitrobenzene and pentanitrobenzene in benzene solution react with hydrogen halides (HCl, HBr, HI, but not HF) at 25 deg C to produce high yields of pentanitrohalobenzenes and 2,3,4,6-tetranitrohalobenzenes, respectively.Pentanitrofluorobenzene also reacts readily with HCl to yield 3-chloro-2,4,5,6-tetranitrofluorobenzene, but the other pentanitrohalobenzenes are much less reactive. 1,2,3,5- and 1,2,4,5-tetranitrobenzenes react rapidly with concentrated hydrochloric or hydrobromic acids at reflux to form picryl halides and 1-halo-2,4,5-trinitrobenzenes, respectively; pentanitrotoluene reacts very slowly under these conditions to form 3-halo-2,4,5,6-tetranitrotoluenes in lower yields.The scope and limitations of this regioselective reaction are defined, and comparison is made to related reactions.A mechanism is presented and discussed.

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