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111599-07-6

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111599-07-6 Usage

Description

(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile is a chemical compound with the molecular formula C11H14N2. It is a derivative of isoquinoline, a heterocyclic aromatic compound. (1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile appears as a colorless liquid and is used in various chemical reactions and organic synthesis. It has been studied for its potential pharmacological properties, particularly its role as a central nervous system stimulant. Additionally, it has shown potential in the development of pharmaceutical drugs due to its unique chemical structure and reactivity. Overall, (1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile has garnered interest in both the scientific and industrial communities for its diverse applications and potential biological activities.

Uses

Used in Chemical Reactions and Organic Synthesis:
(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile is used as a chemical intermediate for various chemical reactions and organic synthesis processes. Its unique chemical structure and reactivity make it a valuable component in the synthesis of other compounds.
Used in Pharmaceutical Development:
(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile is used as a potential candidate in the development of pharmaceutical drugs. Its unique chemical structure and reactivity contribute to its potential as a central nervous system stimulant and its potential use in the treatment of various medical conditions.
Used in Research and Development:
(1,2,3,4-Tetrahydro-isoquinolin-1-yl)-acetonitrile is used as a subject of research and development in both the scientific and industrial communities. Its diverse applications and potential biological activities make it an interesting compound for further study and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 111599-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111599-07:
(8*1)+(7*1)+(6*1)+(5*5)+(4*9)+(3*9)+(2*0)+(1*7)=116
116 % 10 = 6
So 111599-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2/c12-7-5-11-10-4-2-1-3-9(10)6-8-13-11/h1-4,11,13H,5-6,8H2

111599-07-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,2,3,4-tetrahydroisoquinolin-1-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names HMS1637P01

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:111599-07-6 SDS

111599-07-6Downstream Products

111599-07-6Relevant articles and documents

Copper-Catalyzed Cyanomethylation of Substituted Tetrahydroisoquinolines with Acetonitrile

Zhang, Wei,Yang, Shiping,Shen, Zengming

, p. 2392 - 2397 (2016/08/16)

A novel method for the synthesis of cyanomethylated tetrahydroisoquinolines has been developed with mild reaction conditions, good yields and a broad substrate scope. Acetonitrile, a common solvent, is for the first time used as a pronucleophile for this type of two sp3C?H bonds cross-dehydrogenative coupling (CDC) reaction. A new oxidative system (CuCl2/TEMPO/Cs2CO3) has been established by our group, in which the mild TEMPO reagent was found to be a highly efficient oxidant. (Figure presented.).

The Reaction of 3,4-Dihydroisoquinolines With Malonic Acid and Its Derivatives

Pelletier, Jeffrey C.,Cava, Michael P.

, p. 474 - 477 (2007/10/02)

The reaction of various 3,4-dihydroisoquinolines with malonic acid gives the corresponding 1,2,3,4-tetrahydro-1-isoquinolineacetic acids in good yield, while the reaction with cyanoacetic acid and malonic acid half ethyl ester affords 1,2,3,4-tetrahydro-1

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