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40662-43-9

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40662-43-9 Usage

Description

2-Cyano-2-propanol-1,1,1,3,3,3-D6, with the CAS number 40662-43-9, is a deuterated organic compound characterized by its oil-like chemical properties. It is primarily utilized in the field of organic synthesis, where its unique structure and deuterium labeling contribute to various chemical reactions and processes.

Uses

Used in Organic Synthesis:
2-Cyano-2-propanol-1,1,1,3,3,3-D6 is used as a synthetic building block for the creation of a wide range of organic compounds. Its application in organic synthesis is due to its versatile structure, which allows for the formation of various functional groups and molecular frameworks.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyano-2-propanol-1,1,1,3,3,3-D6 is used as a key intermediate in the development of new drugs. Its deuterated nature can provide isotopically labeled compounds, which are valuable for studying the metabolic pathways and pharmacokinetics of drug candidates.
Used in Chemical Research:
2-Cyano-2-propanol-1,1,1,3,3,3-D6 is also employed in chemical research as a tool to investigate reaction mechanisms and to understand the role of deuterium in various chemical processes. Its use in research helps to advance the knowledge of chemical reactions and the development of novel synthetic methods.
Used in Material Science:
In the field of material science, 2-Cyano-2-propanol-1,1,1,3,3,3-D6 can be used as a component in the synthesis of advanced materials with specific properties. Its incorporation into polymers or other materials can lead to improved performance characteristics, such as enhanced stability or altered physical properties.
Overall, 2-Cyano-2-propanol-1,1,1,3,3,3-D6 is a valuable compound with diverse applications across various industries, including organic synthesis, pharmaceuticals, chemical research, and material science. Its unique properties and deuterium labeling make it an essential tool for the development of new compounds and the advancement of scientific knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 40662-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,6 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40662-43:
(7*4)+(6*0)+(5*6)+(4*6)+(3*2)+(2*4)+(1*3)=99
99 % 10 = 9
So 40662-43-9 is a valid CAS Registry Number.

40662-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Cyano-2-propanol-1,1,1,3,3,3-d6

1.2 Other means of identification

Product number -
Other names 3,3,3-trideuterio-2-hydroxy-2-(trideuteriomethyl)propanenitrile

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:40662-43-9 SDS

40662-43-9Relevant articles and documents

DEUTERATED MK2 PATHWAY INHIBITORS AND METHODS OF USING THE SAME

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Paragraph 0321, (2021/02/05)

The present disclosure provides deuterated pyridinone-pyridinyl compounds and compositions useful in the treatment of p38 MAP Kinase mediated having the structures of Formula (I); wherein the A, B, and R groups are as defined in the detailed description. Methods of inhibition of p38 MAP Kinase activity in a human or animal subject are also provided.

DERIVATIVES OF RESIQUIMOD

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Paragraph 143; 144, (2018/12/12)

A deuterated compound having structural formula I or a pharmaceutically acceptable salt thereof: Values and example values of the variable in formula (I) are disclosed herein. Also disclosed are the use of compounds of formula (I) in the methods of treating a disease selected from cancer, an autoimmune disease, and an infectious disease, and methods of enhancing an immune response to an antigen.

MANUFACTURING METHOD OF DEUTERATED METHYL METHACRYLATE

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Page/Page column 9, (2010/02/11)

PROBLEM TO BE SOLVED: To provide an economical manufacturing method of methyl methacrylate-d8 (C5D8O2) which is excellent in both the deuteration rate and the chemical purity and is useful as a raw material for plastic optical fibers and optical waveguide materials having a low transmission loss.SOLUTION: Methyl methacrylate-d8 is manufactured using as raw materials readily available methanol-d4 and acetone-d6 with all hydrogen atoms thereof deuterated, where methanol-d4 is converted into methanol-d3 with its methyl group fully deuterated and methyl methacrylate-d8 is obtained from the thus-obtained methanol-d3 with its methyl group fully deuterated and acetone cyanhydrin-d6 prepared from acetone-d6. A deuterium-containing compound, recovered when methanol-d4 is converted into methanol-d3 with its methyl group fully deuterated, is reutilized as a part of raw materials for manufacturing methanol-d4 and acetone-d6.

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