Welcome to LookChem.com Sign In|Join Free
  • or
(1-adamantylamino)acetonitrile, also known as 1-Adamantylamino)acetonitrile, is a chemical compound with the chemical formula C11H18N. It is a derivative of 1-adamantylamine and acetonitrile, and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This white solid at room temperature has a melting point of 103-105 °C and is considered a moderately hazardous substance, requiring careful handling and storage. Its versatility makes it a valuable compound in fields such as medicinal chemistry, material science, and organic synthesis.

16782-40-4

Post Buying Request

16782-40-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

16782-40-4 Usage

Uses

Used in Pharmaceutical Industry:
(1-adamantylamino)acetonitrile is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drug molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the realm of organic synthesis, (1-adamantylamino)acetonitrile is utilized as a building block for creating a wide range of organic compounds, showcasing its reactivity and structural properties.
Used in Material Science:
(1-adamantylamino)acetonitrile is employed in material science for the development of new materials with unique properties, such as improved stability or specific interactions, due to its adamantane-based structure and nitrile functional group.

Check Digit Verification of cas no

The CAS Registry Mumber 16782-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16782-40:
(7*1)+(6*6)+(5*7)+(4*8)+(3*2)+(2*4)+(1*0)=124
124 % 10 = 4
So 16782-40-4 is a valid CAS Registry Number.

16782-40-4Relevant academic research and scientific papers

1-(1-Adamantyl)diaziridine

Kuznetsov,Makhova,Chervin,Kostyanovsky

, p. 828 - 829 (1997)

The reaction of 1-aminoadamantane with CH2O and H2NOSO3H in the presence of K2CO3 under phase-transfer conditions leads to hitherto unknown 1-(1-adamantyl)diaziridine and (1-adamantyl)aminoacetonitrile, characterized by spectral data.

A novel transformation of primary amines to N-monoalkylhydroxylamines

Tokuyama,Kuboyama,Amano,Yamashita,Fukuyama

, p. 1299 - 1304 (2007/10/03)

A novel transformation of primary amines to the corresponding N-monoalkylhydroxylamines is described. The three-step protocol involves selective mono-cyanomethylation of primary amines, regioselective formation of nitrones by m-CPBA oxidation, and hydroxylaminolysis of the nitrones with hydroxylamine hydrochloride. The method is applicable for a wide range of primary amines, including alkyl, benzyl, and chiral.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 16782-40-4