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2,4-Hexadienedinitrile, also known as (E,E)-2,4-hexadienedinitrile, is an organic compound with the chemical formula C6H6N2. It is a conjugated diene with two nitrile groups, which are characterized by the presence of a triple bond between carbon and nitrogen. 2,4-Hexadienedinitrile, (E,E)- is a colorless liquid with a pungent odor and is soluble in organic solvents. It is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle 2,4-Hexadienedinitrile, (E,E)- with care, as it can be toxic and may cause irritation to the skin, eyes, and respiratory system.

5867-88-9

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5867-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5867-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5867-88:
(6*5)+(5*8)+(4*6)+(3*7)+(2*8)+(1*8)=139
139 % 10 = 9
So 5867-88-9 is a valid CAS Registry Number.

5867-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name hexa-2t,4t-dienedinitrile

1.2 Other means of identification

Product number -
Other names Hexa-2t,4t-diendinitril

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:5867-88-9 SDS

5867-88-9Upstream product

5867-88-9Relevant academic research and scientific papers

AMMOXYDATION CATALYTIQUE DES HYDROCARBURES ET REACTIONS APPARENTEES. XXII. AMMOXYDATION DU BENZENE ET DU CYCLOHEXANE

Simon, Gerard,Germain, Jean-Eugene

, p. 149 - 155 (2007/10/02)

Benzene ammoxidation at 440-550 deg C/1 at. produces, on V-Mo, Ti-Mo, Bi-Mo (oxides) catalysts, unsaturated C4 (maleo and fumaronitriles) and C6 (mucononitrile and stereoisomers) dinitriles.These initial selectivities fall with increasing conversions, and C6 dinitriles disappear above 10percent conversion by thermal or catalytic degradation.The main initial stereoisomer cis-cis (mucononitrile) is consistent with a 1-2 attack of the aromatic ring, so far unknown in catalytic oxidations.Cyclohexane ammoxidation goes through the oxidative dehydrogenation to benzene and proceduces small amounts of C4 unsaturated dinitriles along with traces of C4, C5 and C6 saturated dinitriles coming from a different reaction path.In both cases, V-Mo and Ti-Mo are the best catalysts for dinitriles production; no C6 formed on Sn-Mo, Sb-Mo and Sn-Sb-Fe-catalysts.

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