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748805-97-2

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748805-97-2 Usage

General Description

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. This chemical is commonly used in organic synthesis and pharmaceutical research as a building block for the production of various pharmaceutical drugs and related compounds. It is also known for its potential pharmacological properties and has been studied for its potential application in medicinal chemistry. Additionally, it has been utilized in the development of new drug candidates and chemical entities for various therapeutic purposes.

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 articles and documents

BTK INHIBITORS

-

, (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.

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.

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.

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