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1-(Tert-butoxycarbonyl)-3-(methanesulfonyloxy)azetidine is an azetidine derivative featuring a tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom and a methanesulfonyloxy group on the carbon atom. This chemical compound is known for its stability and versatility in organic synthesis, particularly in the formation of amine derivatives. The Boc group ensures the nitrogen atom's stability, enabling selective functional group manipulations, while the methanesulfonyloxy group acts as a leaving group in nucleophilic substitution reactions. Its reactivity and synthetic utility make it a valuable component in the development of pharmaceuticals, agrochemicals, and other fine chemicals.

141699-58-3

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141699-58-3 Usage

Uses

Used in Pharmaceutical Development:
1-(Tert-butoxycarbonyl)-3-(methanesulfonyloxy)azetidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the creation of complex amine derivatives, which are essential building blocks in the development of new drugs.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(Tert-butoxycarbonyl)-3-(methanesulfonyloxy)azetidine is utilized as a reagent for the synthesis of amine-containing agrochemicals. Its ability to facilitate complex synthetic transformations contributes to the development of novel and effective agrochemicals for crop protection and pest control.
Used in Fine Chemicals Production:
1-(Tert-butoxycarbonyl)-3-(methanesulfonyloxy)azetidine is employed as a versatile building block in the production of fine chemicals. Its stability and reactivity enable the synthesis of a wide range of specialty chemicals, including chiral compounds, which are important in various industrial applications, such as fragrances, flavors, and pharmaceutical intermediates.
Used in Organic Synthesis Research:
As a reagent in organic synthesis, 1-(Tert-butoxycarbonyl)-3-(methanesulfonyloxy)azetidine is used for exploring new synthetic methodologies and reaction mechanisms. Its unique properties provide opportunities for researchers to investigate novel approaches to the synthesis of amine derivatives and other complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 141699-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141699-58:
(8*1)+(7*4)+(6*1)+(5*6)+(4*9)+(3*9)+(2*5)+(1*8)=153
153 % 10 = 3
So 141699-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO5S/c1-9(2,3)14-8(11)10-5-7(6-10)15-16(4,12)13/h7H,5-6H2,1-4H3

141699-58-3 Well-known Company Product Price

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  • Aldrich

  • (SYX00004)  tert-Butyl 3-[(methylsulfonyl)oxy]-1-azetanecarboxylate  AldrichCPR

  • 141699-58-3

  • SYX00004-1G

  • 966.42CNY

  • Detail

141699-58-3SDS

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-Boc-3-Methanesulfonyloxyazetidine

1.2 Other means of identification

Product number -
Other names tert-Butyl 3-[(methylsulfonyl)oxy]-1-azetanecarboxylate

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:141699-58-3 SDS

141699-58-3Relevant articles and documents

RET Inhibitor. Pharmaceutical composition and use thereof

-

, (2021/10/27)

The invention belongs to the field of medicines, and relates to RET inhibitor, a pharmaceutical composition and application thereof. , The present invention relates to a compound represented by formula (I), a stereoisomer, a tautomer, an oxynitride, a solvate, a metabolite, a pharmaceutically acceptable salt or prodrug thereof, I, and a pharmaceutical composition thereof in the manufacture of a medicament, in particular for the treatment and prophylaxis of diseases and disorders associated and RET.

A novel RET inhibitor. Pharmaceutical composition and use thereof

-

, (2021/11/26)

The invention belongs to the field of medicines, and relates to a novel RET inhibitor, a pharmaceutical composition and application thereof. In particular, the invention relates to a compound represented by formula (I), a stereoisomer, a tautomer, an oxynitride, a solvate, a metabolite, a pharmaceutically acceptable salt or prodrug thereof, I said compound and a pharmaceutical composition thereof for the manufacture of a medicament, in particular for the treatment and prophylaxis and RET of diseases and disorders associated with irritable bowel syndrome.

BROAD-SPECTRUM CARBAPENEMS

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, (2021/05/29)

The present disclosure provides broad-spectrum carbapenem derivatives and pharmaceutical compositions useful in the treatment of bacterial infections and methods for treating such infections using such derivatives and/or compositions.

PROTEIN TYROSINE PHOSPHATASE DEGRADERS AND METHODS OF USE THEREOF

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Page/Page column 170-171, (2021/06/26)

Provided herein are compounds, compositions, and methods useful for degrading protein tyrosine phosphatase, e.g., protein tyrosine phosphatase non-receptor type 2 (PTPN2) and/or protein tyrosine phosphatase non-receptor type 1 (PTPN1), and for treating related diseases favorably responsive to PTPN1 or PTPN2 inhibitor treatment, e.g., a cancer 5 or a metabolic disease.

RET inhibitor and pharmaceutical composition and application thereof

-

Paragraph 0356; 0364-0365, (2021/10/27)

The invention belongs to the field of medicines, and relates to an RET inhibitor and a pharmaceutical composition and application thereof. Specifically, the invention relates to a compound as shown in a formula (I), or a stereoisomer, a tautomer, a nitrogen oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug of the compound as shown in the formula (I). The invention also relates to pharmaceutical compositions comprising the compounds, and uses of the compounds and pharmaceutical compositions thereof in the preparation of a medicine which is especially used for the treatment and prevention of RET-related diseases and disorders, including cancers, irritable bowel syndrome and/or pain associated with irritable bowel syndrome.

RET Inhibitor. Pharmaceutical composition and use thereof

-

Paragraph 0301-0303, (2021/10/27)

The invention belongs to the field of medicines, and relates to RET inhibitor, a pharmaceutical composition and application thereof. , The present invention relates to a compound represented by formula (I), a stereoisomer, a tautomer, an oxynitride, a solvate, a metabolite, a pharmaceutically acceptable salt or prodrug thereof, I, and a pharmaceutical composition thereof in the manufacture of a medicament, in particular for the treatment and prophylaxis of diseases and disorders associated and RET.

RET Inhibitor. Pharmaceutical composition and use thereof

-

Paragraph 0316-0317, (2021/11/26)

The invention belongs to the field of medicines, and relates to a novel RET inhibitor, a pharmaceutical composition and application thereof. , The present invention relates to a compound represented by formula (I), a stereoisomer, a geometric isomer, a tautomer, an oxynitride, a solvate, a metabolite, a pharmaceutically acceptable salt or prodrug thereof, I, and a pharmaceutical composition thereof in the manufacture of a medicament, in particular for the treatment and prevention and RET of diseases and disorders associated with irritable bowel syndrome.

AZETIDINE DERIVATIVE, AND PRODRUG THEREOF

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Paragraph 0143; 0145, (2021/04/16)

An object of the present invention is to provide a compound useful as a therapeutic or prophylactic drug for a disease involving the immune system, by suppressing a function of immune cells by suppressing proliferation of activated T cells or suppressing production of interferon alpha (IFN-α) by activated plasmacytoid dendritic cells (pDC), particularly an autoimmune disease such as systemic lupus erythematosus (SLE) and lupus nephritis in SLE patients. The present invention provides a compound represented by general formula (I) : [wherein X, R1, R2, R3, R4, R5 and R6 are as described in the description], or a pharmaceutically acceptable salt thereof.

ATF6 MODULATORS AND USES THEREOF

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Paragraph 253, (2021/04/17)

Compounds (1-2) as modulators of Activating Transcription Factor 6 (ATF6) are provided. The compounds may find use as therapeutic agents for the treatment of diseases or disorders mediated by ATF6 and may find particular use in the treatment of viral infections, neurodegenerative diseases, vascular diseases, or cancer. (Formula (1-2))

AZAINDOLE DERIVATIVE AND USE THEREOF AS FGFR AND C-MET INHIBITOR

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Paragraph 0134, (2021/05/29)

A series of pyrazolopymidine derivatives, and use thereof in the preparation of a medicament for treating disease associated with FGFR and c-Met. The pyrazolopymidine derivative is a compound represented by formula (I), a tautomer, or a pharmaceutically acceptable salt thereof.

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