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2-Boc-2,6-diazabicyclo[3.2.0]heptane is an organic compound that features a bicyclic structure with a Boc-protecting group and a nitrogen atom at the 2nd position. It is a versatile building block in organic synthesis and has potential applications in the pharmaceutical industry due to its unique structure and reactivity.

1204405-68-4

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1204405-68-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Boc-2,6-diazabicyclo[3.2.0]heptane is used as a reagent for the preparation of pyrimidine derivatives, which are crucial in the development of KRas G12C inhibitors. These inhibitors are designed to target and treat KRas-mediated diseases, such as certain types of cancer, by specifically inhibiting the mutated KRas G12C protein.
The compound's utility in the synthesis of pyrimidine derivatives highlights its importance in the development of novel therapeutic agents for the treatment of KRas-mediated diseases, making it a valuable asset in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1204405-68-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,4,0 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1204405-68:
(9*1)+(8*2)+(7*0)+(6*4)+(5*4)+(4*0)+(3*5)+(2*6)+(1*8)=104
104 % 10 = 4
So 1204405-68-4 is a valid CAS Registry Number.

1204405-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4,7-diazabicyclo[3.2.0]heptane-4-carboxylate

1.2 Other means of identification

Product number -
Other names 2-BOC-2,6-DIAZABICYCLO[3.2.0]HEPTANE

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:1204405-68-4 SDS

1204405-68-4Relevant academic research and scientific papers

QUINAZOLINE COMPOUNDS, PREPARATION METHODS AND USES THEREOF

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Paragraph 285; 288, (2022/01/12)

Provided herein are novel compounds, for example, compounds having a Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt thereof. Also provided herein are methods of preparing the compounds and methods of using the compounds, for example, in inhibiting KRAS G12D in a cancer cell, and/or in treating various cancer such as pancreatic cancer, colorectal cancer, lung cancer or endometrial cancer.

KRAS G12C INHIBITORS

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Paragraph 0399, (2020/07/25)

The present invention relates to compounds that inhibit KRas G12C. In particular, the present invention relates to compounds that irreversibly inhibit the activity of KRas G12C, pharmaceutical compositions comprising the compounds and methods of use therefor.

Substituted diazabicycloalkane derivatives

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Page/Page column 36, (2010/02/11)

Compounds of formula (I) [in-line-formulae]Z-Ar1—Ar2??(I) [/in-line-formulae] wherein Z is a diazabicyclic amine, Ar1 is a 5- or 6-membered aromatic ring, and Ar2 is selected from the group consisting of an unsubstituted or substituted 5- or 6-membered heteroaryl ring; unsubstituted or substituted bicyclic heteroaryl ring; 3,4-(methylenedioxy)phenyl; carbazolyl; tetrahydrocarbazolyl; naphthyl; and phenyl; wherein the phenyl is substituted with 0, 1, 2, or 3 substituents in the meta- or para-positions. The compounds are useful in treating conditions or disorders prevented by or ameliorated by α7 nAChR ligands. Also disclosed are pharmaceutical compositions comprising compounds of formula (I) and methods for using such compounds and compositions.

Diazabicyclic central nervous system active agents

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, (2008/06/13)

Compounds of formula I pharmaceutical compositions of these compounds, and use of said compositions to control synaptic transmission in mammals.

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