79996-90-0

Basic information

• Product Name: 4-(HYDROXYMETHYL)NAPHTHALENE-1-CARBONITRILE
• Synonyms: 4-(HYDROXYMETHYL)NAPHTHALENE-1-CARBONITRILE;4-(hydroxymethyl)-1-naphthonitrile
• CAS NO: 79996-90-0
• Molecular Formula: C₁₂H₉NO
• Molecular Weight: 183.21
• Mol File: 79996-90-0.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-(HYDROXYMETHYL)NAPHTHALENE-1-CARBONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(HYDROXYMETHYL)NAPHTHALENE-1-CARBONITRILE(79996-90-0)
• EPA Substance Registry System: 4-(HYDROXYMETHYL)NAPHTHALENE-1-CARBONITRILE(79996-90-0)

Safety Data

• Hazardous Substances Data: 79996-90-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-(Hydroxymethyl)naphthalene-1-carbonitrile is utilized as a key intermediate in organic synthesis for the production of a wide range of organic compounds. Its unique structure allows for various chemical reactions, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Hydroxymethyl)naphthalene-1-carbonitrile is used as a precursor in the development of new drugs. Its chemical properties enable the creation of novel drug candidates with potential therapeutic applications.
Used in Dye Production:
4-(Hydroxymethyl)naphthalene-1-carbonitrile is employed as a starting material in the synthesis of various dyes. Its ability to form different chemical structures contributes to the development of new dyes with unique color properties and applications.
Used in Materials Science:
In the field of materials science, 4-(Hydroxymethyl)naphthalene-1-carbonitrile may have potential applications as a precursor for the preparation of various functional materials. Its versatility in chemical reactions allows for the development of materials with specific properties tailored for various applications.
Overall, 4-(Hydroxymethyl)naphthalene-1-carbonitrile is a versatile chemical compound with a wide range of applications in organic synthesis, pharmaceuticals, dyes, and materials science. Its unique structure and chemical properties make it a valuable building block for the development of new and innovative products.

Upstream product

• 67-56-1 methanol 
• 3029-30-9 naphthalene-1,4-dicarbonitrile 
• 101-81-5 Diphenylmethane 
• 108-88-3 toluene 

Downstream Products

• 76454-99-4 2,3-dimethyl-2-butenyl (1-cyano-4-naphthyl)methyl ether 
• 94719-68-3 2,4,5-trimethylbenzyl-(1-cyano-4-naphthyl)-methyl ether 
• 145224-19-7 Benzoic acid 4-cyano-naphthalen-1-ylmethyl ester 
• 41014-20-4 4-bromomethyl-1-naphthonitrile 
• 94719-67-2 4-methylbenzyl-(1-cyano-4-naphthyl)methyl ether 
• 123674-43-1 4-cyano-1-naphthylmethyl phenylacetate 
• 145224-20-0 4-Methoxy-benzoic acid 4-cyano-naphthalen-1-ylmethyl ester 

Relevant articles and documents

Set Photochemical Reactions between 1,4-Naphthalenedicarbonitrile and Benzylic Donors. Medium Effects

The electron transfer induced photochemical reactions 1,4-naphthalenedicarbonitrile (NDN) with toluene (1a), diphenylmethane (1b), p-methoxytoluene (1c), and benzyltrimethylsilane (1d) in MeOH-MeCN and 0.1 M KOH-MeOH-MeCN were examined.The results were compared with those of reactions occurring in neat MeCN.Under the former conditions, the cation radical derived from 1a undergoes deprotonation after diffusion from (rather than within) the geminate ion pair (as in MeCN).The formed benzyl radical abstracts a hydrogen from MeOH leading to hydroxymethylation of NDN competitively with its benzylation.Under basis conditions MeO(-) adds to 1a(+.) yielding 1c.The reaction of 1b in MeOH-MeCN and 0.1 M KOH-MeOH-MeCN is similar to that of 1a.However, in the reaction of 1c under these conditions, the arene cation radical undergoes deprotonation out of cage.Finally, desilylation of the cation radical from 1d is a fast process occurring from the geminate pair in all the media explored.