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148404-28-8

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148404-28-8 Usage

General Description

N-BOC-HEXAHYDRO-5-OXOCYCLOPENTA[C]PYRROLE is a chemical compound that belongs to the class of pyrrole derivatives. It is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and biologically active molecules. The compound consists of a hexahydro-5-oxocyclopenta[c]pyrrole core structure with a BOC (tert-butyloxycarbonyl) protecting group attached to the amine functional group. This protecting group helps to stabilize and control the reactivity of the amine group during chemical reactions. N-BOC-HEXAHYDRO-5-OXOCYCLOPENTA[C]PYRROLE has applications in the development of drugs and advanced materials due to its versatile reactivity and structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 148404-28-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,0 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 148404-28:
(8*1)+(7*4)+(6*8)+(5*4)+(4*0)+(3*4)+(2*2)+(1*8)=128
128 % 10 = 8
So 148404-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H19NO3/c1-12(2,3)16-11(15)13-6-8-4-10(14)5-9(8)7-13/h8-9H,4-7H2,1-3H3

148404-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-Hexahydro-5-oxocyclopenta[c]pyrrole

1.2 Other means of identification

Product number -
Other names N-Boc-hexahydro-5-oxocyclopenta[c]pyrrole

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:148404-28-8 SDS

148404-28-8Relevant articles and documents

Ternary fused ring substituted six-membered ring derivatives and their use in medicine

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Paragraph 0195-0197, (2019/01/22)

The invention relates to a fused tricyclic substituted amino six-membered ring derivative and application thereof in medicine, particularly a fused tricyclic substituted amino six-membered ring derivative shown in a formula (I) or stereoisomers and pharmaceutically acceptable salts or pro-drugs of the derivative, a pharmaceutical composition comprising the derivative and use of the derivative in preparing a dipeptidyl peptidase IV (DPP-IV) inhibitor in medicine, wherein the substituents in the formula (I) are defined as in the description. The formula (I) is shown in the description.

SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE

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, (2017/03/28)

The present invention provides novel heteroaryl compounds, pharmaceutical acceptable salts and formulations thereof. They are useful in preventing, managing, treating or lessening the severity of a protein kinase-mediated disease. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of protein kinase-mediated disease.

Three-membered fused ring substituted amino six-membered ring derivative and medicine applications thereof relates to a three-membered fused ring substituted amino six-membered ring derivative as shown in the general formula

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Page/Page column 33; 34, (2017/08/02)

The present invention relates to a three-membered fused ring substituted amino six-membered ring derivative and medicine applications thereof, and more particularly to a three-membered fused ring substituted amino six-membered ring derivative as shown in the general formula (I) or a stereoisomer of the derivative, a pharmaceutically acceptable salt, a prodrug, a medicinal composition containing the derivative and an application of the derivative to preparation of the medicine, namely a dipeptidyl peptidase IV(DPP-IV) inhibitor, wherein the definitions of the various substituents in the general formula (I) are the same as those in the specification.

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