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741287-46-7

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741287-46-7 Usage

Description

1-Boc-4-Isopropylpiperazine, also known as Boc-IPPA, is a chemical compound with the formula C13H27N3O2. It is an organic compound that is commonly used as a building block in the synthesis of various pharmaceuticals and other organic compounds. Boc-IPPA is a piperazine derivative, and its structure contains a Boc (tert-butoxycarbonyl) protecting group, which is commonly used in organic synthesis to protect reactive functional groups. 1-Boc-4-Isopropylpiperazine has potential applications in medicinal chemistry and drug development due to its ability to modulate biological processes, and it is an important intermediate in the synthesis of various pharmaceuticals. Additionally, Boc-IPPA is also used in the synthesis of materials for various applications in the chemical industry. Overall, 1-Boc-4-Isopropylpiperazine is a versatile chemical compound with valuable applications in organic synthesis and pharmaceutical research.

Uses

Used in Pharmaceutical Industry:
1-Boc-4-Isopropylpiperazine is used as a building block for the synthesis of various pharmaceuticals for its ability to modulate biological processes and serve as an important intermediate in the development of new drugs.
Used in Chemical Industry:
1-Boc-4-Isopropylpiperazine is used in the synthesis of materials for various applications, such as the production of specialty chemicals and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 741287-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,2,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 741287-46:
(8*7)+(7*4)+(6*1)+(5*2)+(4*8)+(3*7)+(2*4)+(1*6)=167
167 % 10 = 7
So 741287-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H24N2O2/c1-10(2)13-6-8-14(9-7-13)11(15)16-12(3,4)5/h10H,6-9H2,1-5H3

741287-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-propan-2-ylpiperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-isopropylpiperazine-4-carboxylic acid tert-butyl ester

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:741287-46-7 SDS

741287-46-7Relevant articles and documents

Discovery of a Novel Mycobacterial F-ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines

Anbarasu, Sivaraj,Bates, Roderick W.,Dick, Thomas,Dr?ge, Peter,Grüber, Gerhard,Harikishore, Amaravadhi,Hotra, Adam,Kalia, Nitin Pal,Kalyanasundaram, Revathy,Lakshmanan, Umayal,Makhija, Harshyaa,Ng, Pearly Shuyi,Parthasarathy, Krupakar,Pethe, Kevin,Poulsen, Anders,Pradeep, Chaudhari Namrata,Ragunathan, Priya,Sae-Lao, Patcharaporn,Sarathy, Jickky Palmae,Saw, Wuan-Geok,Seankongsuk, Pattarakiat,Shin, Joon,Tan, Jocelyn Hui Ling

, p. 13295 - 13304 (2020/06/03)

The F1FO-ATP synthase is required for growth and viability of Mycobacterium tuberculosis and is a validated clinical target. A mycobacterium-specific loop of the enzyme's rotary γ subunit plays a role in the coupling of ATP synthesis within the enzyme complex. We report the discovery of a novel antimycobacterial, termed GaMF1, that targets this γ subunit loop. Biochemical and NMR studies show that GaMF1 inhibits ATP synthase activity by binding to the loop. GaMF1 is bactericidal and is active against multidrug- as well as bedaquiline-resistant strains. Chemistry efforts on the scaffold revealed a dynamic structure activity relationship and delivered analogues with nanomolar potencies. Combining GaMF1 with bedaquiline or novel diarylquinoline analogues showed potentiation without inducing genotoxicity or phenotypic changes in a human embryonic stem cell reporter assay. These results suggest that GaMF1 presents an attractive lead for the discovery of a novel class of anti-tuberculosis F-ATP synthase inhibitors.

NOVEL PROCESSES FOR THE PREPARATION OF CYCLOPROPYL-AMIDE DERIVATIVES

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Page/Page column 49, (2010/11/27)

The present invention is directed to novel processes for the preparation of cyclopropyl-amide derivatives, useful for the treatment of disorders and conditions mediated by the histamine receptor.

PYRAZOLE DERIVATIVE

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Page/Page column 64, (2008/06/13)

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