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2-bromo-1,3-diiodo-5-nitrobenzene is an organic compound characterized by its molecular formula C6H2BrI2NO2. 2-bromo-1,3-diiodo-5-nitrobenzene features a benzene ring with a bromine atom at the 2-position, two iodine atoms at the 1 and 3 positions, and a nitro group at the 5-position. It is a halogenated aromatic compound, which means it contains multiple halogen atoms (bromine and iodine) attached to the benzene ring. The presence of the nitro group imparts specific chemical properties, such as increased reactivity and potential to form explosive compounds. Due to its unique structure, 2-bromo-1,3-diiodo-5-nitrobenzene has potential applications in various chemical reactions and synthesis processes, particularly in the fields of pharmaceuticals and materials science.

6311-50-8

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6311-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6311-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6311-50:
(6*6)+(5*3)+(4*1)+(3*1)+(2*5)+(1*0)=68
68 % 10 = 8
So 6311-50-8 is a valid CAS Registry Number.

6311-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1,3-diiodo-5-nitrobenzene

1.2 Other means of identification

Product number -
Other names Benzene,2-bromo-1,3-dichloro-5-nitro

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:6311-50-8 SDS

6311-50-8Upstream product

6311-50-8Relevant academic research and scientific papers

Palladium-Catalyzed Alkenylation and Alkynylation of Polyhaloarenes

Tao, Weijin,Nesbitt, Stephanie,Heck, Richard F.

, p. 63 - 69 (2007/10/02)

Alkenylation of several polyhaloarenes proceeded in low to moderate yields.Iodo groups could be reacted selectively in the presence of bromo groups; however, no more than two alkenyl groups could be introduced on contiguous, aromatic carbons.Alkynylation

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