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1-[(4-chlorophenyl)amino]cyclopentanecarbonitrile is a chemical compound with the molecular formula C12H13ClN2. It is a derivative of cyclopentane, featuring a 4-chlorophenylamine group attached to the cyclopentane ring and a nitrile functional group. 1-[(4-chlorophenyl)amino]cyclopentanecarbonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its unique structure allows for the exploration of different chemical reactions and modifications, making it a valuable intermediate in organic chemistry.

6340-83-6

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6340-83-6 Usage

Type of Compound

Chemical compound

Neuroprotective

It helps protect nerve cells from damage.

Anticonvulsant

It prevents or reduces the severity of seizures.

Mood-stabilizing

It helps regulate mood swings.

Treatment of amyotrophic lateral sclerosis (ALS)

A disease that affects nerve cells in the brain and spinal cord.

Investigational use for other neurodegenerative disorders

Such as Alzheimer's disease and Parkinson's disease.

Mechanism of Action

Reduces the release of glutamate, a neurotransmitter associated with nerve cell damage in ALS.

Administration

Typically administered orally (by mouth).

Effects

Improves survival and delays the need for ventilator support in patients with ALS.

Check Digit Verification of cas no

The CAS Registry Mumber 6340-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6340-83:
(6*6)+(5*3)+(4*4)+(3*0)+(2*8)+(1*3)=86
86 % 10 = 6
So 6340-83-6 is a valid CAS Registry Number.

6340-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chloroanilino)cyclopentane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:6340-83-6 SDS

6340-83-6Relevant academic research and scientific papers

Synthesis of α-aminonitriles under mild catalytic, metal-free conditions

Nammalwar, Baskar,Fortenberry, Chelsea,Bunce, Richard A.

supporting information, p. 379 - 381 (2014/01/06)

α-Aminonitriles have been synthesized by a Strecker synthesis from aldehydes and ketones under mild catalytic, metal-free conditions. Aromatic aldehydes (1 equiv) were reacted with aromatic and 1 or 2 aliphatic amines (1 equiv) in EtOH containing 3 mol %

Synthesis of new imidazolidinones, spiro-imidazolidinones and spiro-hydantoins

Chande, Madhukar S.,Balel, Satish K.

, p. 377 - 380 (2007/10/03)

α-Alkyl/aryl-α-arylaminopropionitriles (1) and 1-arylamino-1-cyano-cyclohexanes/cyclopentanes (5) react with alkyl/arylisocyanates to afford new imidazolidinones (2, 3) and spiro-imidazolidinones (6, 7) respectively. Compounds 2 and 6 on hydrolysis give hydantoins (4) and spiro-hydantoins (8), respectively.

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