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Tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate is a chemical compound with the molecular formula C11H17NO4. It belongs to the oxazepane class of compounds and is derived from tert-butyl carboxylate. tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate is characterized by its unique structure and properties, making it a valuable building block in organic synthesis and pharmaceutical research.

748805-97-2

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748805-97-2 Usage

Uses

Used in Organic Synthesis:
Tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate is used as a building block in organic synthesis for the production of various pharmaceutical drugs and related compounds. Its unique structure allows for the formation of diverse chemical entities, contributing to the development of new and innovative molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate is utilized as a key intermediate in the synthesis of drug candidates. Its potential pharmacological properties have been studied extensively, making it a promising candidate for the development of new therapeutic agents.
Used in Medicinal Chemistry:
Tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate is employed in medicinal chemistry for the exploration of its potential applications in the treatment of various diseases and conditions. Its unique structure and properties have been investigated for their ability to modulate biological targets and pathways, offering new avenues for drug discovery and development.
Used in Drug Development:
In the development of new drug candidates and chemical entities, tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate plays a crucial role. Its versatility and potential pharmacological properties make it an attractive starting point for the design and synthesis of novel therapeutic agents, targeting a wide range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 748805-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,8,8,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 748805-97:
(8*7)+(7*4)+(6*8)+(5*8)+(4*0)+(3*5)+(2*9)+(1*7)=212
212 % 10 = 2
So 748805-97-2 is a valid CAS Registry Number.

748805-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 6-oxo-1,4-oxazepane-4-carboxylate

1.2 Other means of identification

Product number -
Other names N-Boc-6-oxo-1,4-oxazepane

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:748805-97-2 SDS

748805-97-2Relevant academic research and scientific papers

BTK INHIBITORS

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, (2022/02/15)

Provided are compounds of Formula (I): or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R7, R8, R9, A1, A2, Q1, Q2, Q3, A, Z, m and n are as defined herein; pharmaceutical compositions comprising said compounds or pharmaceutically acceptable salts thereof, and pharmaceutically acceptable excipients; and methods of treating a disorder responsive to inhibition of Bruton's tyrosine kinase using said compounds, or pharmaceutically acceptable salts thereof, or said pharmaceutical compositions.

P2X3 MODULATORS

-

Paragraph 00263, (2021/08/20)

Provided herein are P2X3 modulators and methods of utilizing P2X3 modulators in the treatment of diseases, disorders, or conditions. Also described herein are pharmaceutical compositions containing such compounds.

An investigation into the role of 2,6-lutidine as an additive for the RuCl3-NaIO4 mediated oxidative cleavage of olefins to ketones

Watson, David W.,Gill, Matthew,Kemmitt, Paul,Lamont, Scott G.,Popescu, Mihai V.,Simpson, Iain

supporting information, p. 4479 - 4482 (2018/11/23)

2,6-Lutidine has been identified as a beneficial additive for the oxidative cleavage of olefins to ketones by NaIO4 in the presence of catalytic RuCl3, improving the yield and shortening the reaction times. In the absence of 2,6-lutidine reactions stalled at the diol intermediate with incomplete conversion to the desired ketones. The reaction protocol described herein also avoids the use of harmful solvents such as CCl4 and DCE and is tolerant of a range of functional groups.

DUAL NAV1.2/5HT2A INHIBITORS FOR TREATING CNS DISORDERS

-

Paragraph 0252, (2018/03/28)

Compounds of formula I: I are disclosed, as are pharmaceutical compositions containing such compounds. Methods of treating neurological or psychiatric disorders in a patient in need are also disclosed. Such disorders include depression, bipolar disorder, pain, schizophrenia, obsessive compulsive disorder, addiction, social disorder, attention deficit hyperactivity disorder, an anxiety disorder, autism, a cognitive impairment, or a neuropsychiatric symptom such as apathy, depression, anxiety, psychosis, aggression, agitation, impulse control disorders, and sleep disorders in neurological disorders such as Alzheimer's and Parkinson's diseases.

AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

-

, (2015/07/22)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

-

, (2015/09/22)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

BRUTON'S TYROSINE KINASE INHIBITORS

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, (2014/05/24)

Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (BTK). Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the BTK inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions. (Formula I)

BRUTON'S TYROSINE KINASE INHIBITORS

-

, (2011/04/14)

The present invention provides compounds useful as inhibitors of Btk, compositions thereof, and methods of using the same.

TRIAZOLE COMPOUNDS USEFUL IN THERAPY

-

Page 68, (2010/02/08)

A compound of formula (I), or a pharmaceutically acceptable derivative thereof, wherein V represents -(CH2)d(O)e-, -CO-, or -CH(C1-6 alkyl)-; W is -0-, -S(O)a , or -N(R1')-R1 rep

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