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4-Aminocyclohexanecarbonitrile, also known as ACAC, is a chemical compound with the molecular formula C7H11N. It is a colorless to pale yellow liquid under ambient conditions and is commonly used as a precursor for the synthesis of other organic compounds, especially in the pharmaceutical industry. ACAC is a versatile building block for the production of various drugs, including anticancer and antiviral medications. It is known for its ability to participate in a variety of chemical reactions, making it a valuable intermediate in the synthesis of complex organic molecules. However, ACAC is also a hazardous chemical and should be handled with care due to its toxic and potentially harmful effects on human health and the environment.

23083-48-9

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23083-48-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Aminocyclohexanecarbonitrile is used as a precursor for the synthesis of various drugs, particularly in the production of anticancer and antiviral medications. Its versatility in participating in a range of chemical reactions makes it a valuable intermediate in the synthesis of complex organic molecules.
Used in Organic Synthesis:
4-Aminocyclohexanecarbonitrile is used as a versatile building block for the synthesis of other organic compounds. Its ability to participate in various chemical reactions allows it to be a key component in the creation of a wide array of organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 23083-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23083-48:
(7*2)+(6*3)+(5*0)+(4*8)+(3*3)+(2*4)+(1*8)=89
89 % 10 = 9
So 23083-48-9 is a valid CAS Registry Number.

23083-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-aminocyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-Cyano-4-aminocyclohexan

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:23083-48-9 SDS

23083-48-9Downstream Products

23083-48-9Relevant academic research and scientific papers

FUSED HETEROCYCLIC DERIVATIVES, THEIR PREPARATION METHODS THEREOF AND MEDICAL USES THEREOF

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Paragraph 0246; 0252; 0586; 0593-0595, (2019/07/03)

The present invention relates to fused heterocyclic derivatives, processes for their preparation and their use in medicine. Specifically, the present invention relates to a novel derivative represented by the formula (I′), or its pharmaceutically acceptable salt thereof, a pharmaceutical composition containing the derivative or its pharmaceutically acceptable salt thereof, and the method for preparing the derivative and its pharmaceutically acceptable salt thereof. The present invention also relates to the use of the derivative and its pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the derivative and its pharmaceutically acceptable salt thereof in the preparation of medicines, in particularly as IDO inhibitor medicines, for treating and/or preventing cancers. Wherein each substituent of the formula (I′) is the same as defined in the specification.

Corresponding amine nitrile and method of manufacturing thereof

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Paragraph 0143-0147; 0158; 0180; 0191; 0213; 0224, (2017/10/22)

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.

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