1772-25-4 Usage
Description
1,3,6-Hexanetricarbonitrile is an organic compound with the chemical formula C9H5N3. It is a colorless to pale yellow liquid with a characteristic odor. 1,3,6-Hexanetricarbonitrile is known for its high boiling point and unique chemical properties, making it a versatile building block in various chemical reactions and applications.
Uses
Used in Organic Synthesis:
1,3,6-Hexanetricarbonitrile is used as an intermediate in organic synthesis for the production of various chemical compounds. Its reactivity and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used as a High Boiling Point Solvent:
Due to its high boiling point, 1,3,6-Hexanetricarbonitrile is used as a solvent in various industrial processes. It is particularly useful in applications where high temperatures are required, such as in the synthesis of polymers and other high molecular weight compounds.
Used as an Additive to Electrolytes:
1,3,6-Hexanetricarbonitrile is also used as an additive in electrolytes for batteries and other electrochemical applications. Its unique properties contribute to improved performance and stability of the electrolyte, enhancing the overall efficiency and lifespan of the device.
Flammability and Explosibility
Notclassified
Synthesis
Preparation
of 1,3,6-hexanetricarbonitrile: To a solution of 1,6-dicyano-2-butylene
(1,6-dicyano-2-butylene) ) And HCI methyl alcohol solution were reacted
at 40-60 ° C for 4-6h, NaCN was added and the reaction was carried out
at 40-101 ° C to obtain 1,3,6-hexanetricarbonitrile.
Check Digit Verification of cas no
The CAS Registry Mumber 1772-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1772-25:
(6*1)+(5*7)+(4*7)+(3*2)+(2*2)+(1*5)=84
84 % 10 = 4
So 1772-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N3/c10-6-2-1-4-9(8-12)5-3-7-11/h9H,1-5H2
1772-25-4Relevant articles and documents
Novel method for preparing aliphatic tricarbonitrile and aliphatic tricarbonitrile prepared by method
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Paragraph 0075-0089, (2020/08/29)
The invention belongs to the technical field of organic synthesis, and particularly relates to a novel method for preparing aliphatic tricarbonitrile and the aliphatic tricarbonitrile prepared by thenovel method. The novel method for preparing aliphatic tricarbonitrile in the invention comprises the following step: removing COOCbHcXd from a compound II to obtain aliphatic tricarbonitrile. The structure formula of the compound II is as described in the specification; and in the structure formula, a is an integer from 3 to 12, b is greater than or equal to 1, c is greater than or equal to 1, dis greater than or equal to 0, e is 2, and X is a heteroatom. The method is simple to operate, uses easily available raw materials, realizes environmental protection, has great implementation value and social and economic benefits, overcomes the safety problems of aliphatic trinitrile preparation under the condition of sodium in a traditional process, and is high in yield and product purity.
Process for producing aliphatic tricarbonitriles
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, (2008/06/13)
The present invention relates to a process for producing tricarbonitriles corresponding to formula I wherein n is an integer from 2 to 11 by forming an intermediate in the presence of a strong base in a first stage from an aliphatic α-ω-dinitrile corresponding to formula II wherein n is an integer from 3 to 12, and reacting the intermediate in a second stage to form a trinitrile corresponding to formula I by the addition of acrylonitrile.