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3-Nitro-2-hexene is an organic compound with the chemical formula C6H11NO2. It is a colorless liquid with a molecular weight of 127.16 g/mol. 3-Nitro-2-hexene is characterized by the presence of a nitro group (-NO2) attached to the third carbon atom and a double bond between the second and third carbon atoms in a hexene chain. 3-Nitro-2-hexene is synthesized through the nitration of 2-hexene, a process that involves the reaction of the alkene with a mixture of nitric acid and sulfuric acid. It is used as an intermediate in the production of various chemicals, such as pharmaceuticals and dyes, due to its reactive nitro group and double bond. However, it is important to note that 3-nitro-2-hexene is a hazardous substance and should be handled with care due to its potential to cause irritation and other health effects.

6065-16-3

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6065-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6065-16-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6065-16:
(6*6)+(5*0)+(4*6)+(3*5)+(2*1)+(1*6)=83
83 % 10 = 3
So 6065-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-3-5-6(4-2)7(8)9/h4H,3,5H2,1-2H3/b6-4-

6065-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-nitrohex-2-ene

1.2 Other means of identification

Product number -
Other names 2-HEXENE,3-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:6065-16-3 SDS

6065-16-3Downstream Products

6065-16-3Relevant academic research and scientific papers

Efficient and stereoselective nitration of mono- and disubstituted olefins with AgNO2 and TEMPO

Maity, Soham,Manna, Srimanta,Rana, Sujoy,Naveen, Togati,Mallick, Arijit,Maiti, Debabrata

supporting information, p. 3355 - 3358 (2013/04/10)

Nitroolefin is a common and versatile reagent. Its synthesis from olefin is generally limited by the formation of mixture of cis and trans compounds. Here we report that silver nitrite (AgNO2) along with TEMPO can promote the regio- and stereoselective nitration of a broad range of olefins. This work discloses a new and efficient approach wherein starting from olefin, nitroalkane radical formation and subsequent transformations lead to the desired nitroolefin in a stereoselective manner.

A predictably selective nitration of olefin with Fe(NO3) 3 and TEMPO

Naveen, Togati,Maity, Soham,Sharma, Upendra,Maiti, Debabrata

, p. 5949 - 5954 (2013/07/26)

Ferric nitrate with catalytic TEMPO has been identified as a useful reagent for regio- and stereoselective nitration of a wide variety of aromatic, aliphatic, and heteroaromatic olefins. This reaction provided nitroolefins in preparatively useful yields with excellent E-selectivity. Due to its mild nature and operational simplicity, the present protocol is expected to find application in synthetic setup.

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