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4,4-dinitropent-1-ene is an organic compound with the molecular formula C5H6N2O4. It is a yellow, oily liquid that is soluble in organic solvents. This chemical is characterized by the presence of a pentene backbone with two nitro groups (-NO2) attached to the 4th carbon atom. It is an energetic compound, often used in the synthesis of explosives and propellants due to its high energy content. The compound is sensitive to shock and heat, making it potentially hazardous in certain conditions. It is important to handle 4,4-dinitropent-1-ene with care, following proper safety protocols, as it can decompose and release toxic fumes or explode under certain circumstances.

5432-39-3

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5432-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5432-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5432-39:
(6*5)+(5*4)+(4*3)+(3*2)+(2*3)+(1*9)=83
83 % 10 = 3
So 5432-39-3 is a valid CAS Registry Number.

5432-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-dinitropent-1-ene

1.2 Other means of identification

Product number -
Other names 1-Pentene,4,4-dinitro

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:5432-39-3 SDS

5432-39-3Downstream Products

5432-39-3Relevant academic research and scientific papers

PALLADIUM CATALYZED C-ALLYLATION OF NITROALKANES

Aleksandrowicz, Piotr,Piotrowska, Hanna,Sas, Wojciech

, p. 1321 - 1327 (2007/10/02)

A detailed study of palladium catalyzed C-allylation of aliphatic nitro compounds is described.Allylic alcohols and/or their acetates and allyl phenyl ethers were employed as allylating agents.The dependence of the reaction yield on nature and quantity of base and structure of the allylic unit is reported and explained.The lowest yield was obtained for allyl alcohol; however it could be considerably increased by addition of a stoichiometric amount of ethyl acetate.Order of reactivity of functional groups was OPh>OAc>OH.A novel method of synthesis of tetrakis (triphenylphosphine) palladium is also reported.

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