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Tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate is a chemical compound with the molecular formula C12H21NO2S. It is a sulfinyliminoazetidine derivative known for its versatile reactivity and ability to participate in a wide range of chemical reactions. tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate is commonly used as a reagent in organic synthesis and chemical research. Its unique structure, which includes a tert-butyl group, provides stability and sterically hinders unwanted side reactions, making it valuable in the production of pharmaceuticals and other fine chemicals. Tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate also has potential applications in the development of new drugs and materials due to its distinctive properties.

1291487-32-5

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1291487-32-5 Usage

Uses

Used in Organic Synthesis:
Tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate is used as a reagent in organic synthesis for its versatile reactivity and ability to participate in various chemical reactions. Its unique structure allows it to be a valuable component in the production of pharmaceuticals and other fine chemicals.
Used in Chemical Research:
In the field of chemical research, tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate is utilized for its potential to contribute to the understanding of chemical reactions and mechanisms. Its unique properties and reactivity make it an important tool for studying and developing new chemical processes.
Used in Pharmaceutical Production:
Tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate is used as a key component in the production of pharmaceuticals. Its stability and ability to hinder unwanted side reactions make it an essential ingredient in the synthesis of various drugs.
Used in the Development of New Drugs:
Due to its unique structure and properties, tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate has potential applications in the development of new drugs. Its versatility in chemical reactions allows for the exploration of novel drug candidates with potential therapeutic benefits.
Used in the Development of New Materials:
Tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate also has potential applications in the development of new materials. Its unique properties and reactivity can contribute to the creation of innovative materials with various applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1291487-32-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,1,4,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1291487-32:
(9*1)+(8*2)+(7*9)+(6*1)+(5*4)+(4*8)+(3*7)+(2*3)+(1*2)=175
175 % 10 = 5
So 1291487-32-5 is a valid CAS Registry Number.

1291487-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 3-tert-butylsulfinyliminoazetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-Butyl 3-((tert-butylsulfinyl)imino)azetidine-1-carboxylate

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:1291487-32-5 SDS

1291487-32-5Relevant academic research and scientific papers

BENZOFURAN DERIVATIVES FOR THE TREATMENT OF HEPATITIS C

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, (2013/10/21)

The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.

Highly functional group compatible Rh-catalyzed addition of arylboroxines to activated N-tert-butanesulfinyl ketimines

Jung, Hyung Hoon,Buesking, Andrew W.,Ellman, Jonathan A.

supporting information; experimental part, p. 3912 - 3915 (2011/09/16)

The rhodium-catalyzed addition of readily accessible arylboroxines to N-tert-butanesulfinyl ketimines derived from oxetan-3-one, N-Boc-azetidin-3-one, and isatins proceeds in high yields with excellent functional group compatibility. Moreover, high diastereoselectivities are observed for the additions to the N-sulfinyl ketimines derived from isatins.

AKT / PKB INHIBITORS

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Page/Page column 81, (2011/06/11)

The invention relates to a series of compounds with particular activity as inhibitors of the serine-threonine kinase AKT. Also provided are pharmaceutical compositions comprising same as well as methods for treating cancer.

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