40896-74-0 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-Cyanobenzylamine hydrochloride is used as a reagent for the synthesis of various pharmaceutical and agrochemical compounds. Its presence in these industries is crucial for the development of new drugs and agricultural chemicals, contributing to advancements in healthcare and agriculture.
Used in Organic Synthesis:
As a building block in organic synthesis, 3-Cyanobenzylamine hydrochloride is instrumental in the creation of a wide range of biologically active molecules. These molecules have potential applications in various fields, including medicine and biotechnology, where they can be used to develop new treatments and products.
Used in Dye and Pigment Manufacturing:
3-Cyanobenzylamine hydrochloride also serves as a precursor in the manufacture of dyes, pigments, and other fine chemicals. Its role in this industry is vital for the production of high-quality colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Fine Chemical Production:
In the fine chemicals sector, 3-Cyanobenzylamine hydrochloride is utilized as a precursor for the synthesis of specialty chemicals. These fine chemicals are essential in numerous industries, including pharmaceuticals, agriculture, and materials science, where they are used to create high-value products with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 40896-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,9 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40896-74:
(7*4)+(6*0)+(5*8)+(4*9)+(3*6)+(2*7)+(1*4)=140
140 % 10 = 0
So 40896-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2.ClH/c9-5-7-2-1-3-8(4-7)6-10;/h1-4H,5,9H2;1H
40896-74-0Relevant academic research and scientific papers
Catalytic Staudinger Reduction at Room Temperature
Lenstra, Danny C.,Wolf, Joris J.,Mecinovi?, Jasmin
, p. 6536 - 6545 (2019/05/24)
We report an efficient catalytic Staudinger reduction at room temperature that enables the preparation of a structurally diverse set of amines from azides in excellent yields. The reaction is based on the use of catalytic amounts of triphenylphosphine as a phosphine source and diphenyldisiloxane as a reducing agent. Our catalytic Staudinger reduction exhibits a high chemoselectivity, as exemplified by reduction of azides over other common functionalities, including nitriles, alkenes, alkynes, esters, and ketones.
Sustainable organophosphorus-catalysed Staudinger reduction
Lenstra, Danny C.,Lenting, Peter E.,Mecinovi?, Jasmin
, p. 4418 - 4422 (2018/10/17)
A highly efficient and sustainable catalytic Staudinger reduction for the conversion of organic azides to amines in excellent yields has been developed. The reaction displays excellent functional group tolerance to functionalities that are otherwise prone to reduction, such as sulfones, esters, amides, ketones, nitriles, alkenes, and benzyl ethers. The green nature of the reaction is exemplified by the use of PMHS, CPME, and a lack of column chromatography.
