39718-07-5

Basic information

• Product Name: 3,5-DICYANOTOLUENE
• Synonyms: 3,5-DICYANOTOLUENE;5-METHYLISOPHTHALONITRILE;5-Methylisophthalonitrile,97%;3,5-Dicyanotoluene 98%;3,5-DICYANOTOLUENE (5-METHYLISOPHTHALONITRILE);5-Methyl-1,3-benzenedicarbonitrile;5-Methylisophthalonitrile 98%;3,5-Dicyanotoluene, 5-Methylbenzene-1,3-dicarbonitrile
• CAS NO: 39718-07-5
• Molecular Formula: C₉H₆N₂
• Molecular Weight: 142.16
• Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives
• Mol File: 39718-07-5.mol

Chemical Properties

• Melting Point: 166-168°C
• Boiling Point: 276.1°Cat760mmHg
• Flash Point: 128.2°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 0.0049mmHg at 25°C
• Refractive Index: 1.555
• BRN: 1940447
• CAS DataBase Reference: 3,5-DICYANOTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DICYANOTOLUENE(39718-07-5)
• EPA Substance Registry System: 3,5-DICYANOTOLUENE(39718-07-5)

Safety Data

• Hazard Codes: T
• Statements: 22
• Safety Statements: 22-36/37
• RIDADR: 3276
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 39718-07-5(Hazardous Substances Data)

Usage

Uses

Used in Dye and Pigment Production:
3,5-Dicyanotoluene is used as an intermediate in the production of dyes and pigments for its ability to contribute to the color and stability of these compounds. Its chemical structure allows for the creation of a wide range of colorants used in various industries.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3,5-Dicyanotoluene is utilized as a key intermediate in the synthesis of various organic compounds, including active pharmaceutical ingredients. Its reactivity and functional groups make it a valuable component in the development of new drugs.
Used in Organic Compound Synthesis:
3,5-Dicyanotoluene is employed as a building block in the synthesis of other organic compounds, such as polymers and specialty chemicals. Its versatility in chemical reactions enables the production of a diverse array of products with different applications across various industries.

InChI:InChI=1/C9H6N2/c1-7-2-8(5-10)4-9(3-7)6-11/h2-4H,1H3

Upstream product

• 22445-42-7 3,5-dimethylbenzonitrile 
• 557-21-1 zinc(II) cyanide 
• 1611-92-3 3,5-dibromotoluene 
• 13438-29-4 5-methylisophthaloyl dichloride 
• 108-67-8 1,3,5-trimethyl-benzene 
• 499-49-0 5-methylisophthalic aicd 
• 107-46-0 Hexamethyldisiloxane 
• 10365-94-3 1,3,5-tricyanobenzene 
• 90868-23-8 5-methyl-isophthalic acid diamide 

Downstream Products

• 10365-94-3 1,3,5-tricyanobenzene 
• 88779-97-9 2-amino-5-methylbenzene-1,3-dicarbonitrile 
• 453565-57-6 3-cyano-5-methylphenylamidoxime 
• 124289-25-4 α-Bromo-3,5-dicyanotoluene 

Relevant articles and documents

PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

The present invention relates to 2-pyridone derivatives of Formula (I) or (IV) as herein described, compositions containing such compounds, synthetic processes for making such compounds, and therapeutic methods that include the administration of such comp

Kinetics and mechanism of oxidative ammonolysis of mesitylene on a vanadium-titanium oxide catalyst

A staged scheme is proposed for the oxidative ammonolysis of mesitylene on a vanadium-titanium oxide catalyst. Numerical values of the rate constants of the stages were found on a computer on the basis of the condition of minimization of the function of deviations between experimental and calculated values of the observed rates with the aid of the conjugate gradient method.

Photochemical Reaction of Arenecarbonitriles in the Presence of Alkylsilanes, Silyl Ethers and Silyl Amines

The irradiation of benzene-1,2,4,5-tetracarbonitrile, and benzene-1,2,4- as well as benzene-1,3,5-tricarbonitrile in the presence of various tetraalkylsilanes, alkoxytrialkylsilanes, hexamethyldisiloxane or heptamethyldisilazane leads to alkylation of the aromatics.The more substituted alkyl group is selectively fragmented, and the attack takes place at the position(s) of highest spin density in the nitrile radical anion.The reaction involves electron transfer to the nitrile's singlet excited state, and the radical cation appears to cleave mainly in the initial radical ion pair.