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TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE is an amide compound that possesses proteolysis-inducing action. It has potential medicinal applications due to its ability to induce proteolysis, which can be beneficial in various therapeutic areas.

893566-75-1

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893566-75-1 Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE is used as a pharmaceutical agent for its proteolysis-inducing action. This property can be utilized in the development of drugs targeting specific diseases where proteolysis plays a crucial role in the disease progression or treatment.
Used in Medicinal Chemistry Research:
TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE serves as a valuable compound in medicinal chemistry research. Its unique structure and proteolysis-inducing action make it a promising candidate for further investigation and development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 893566-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,5,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 893566-75:
(8*8)+(7*9)+(6*3)+(5*5)+(4*6)+(3*6)+(2*7)+(1*5)=231
231 % 10 = 1
So 893566-75-1 is a valid CAS Registry Number.

893566-75-1SDS

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 8-bromo-3,4-dihydroisoquinoline-2(1H)-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 8-bromo-3,4-dihydro-1H-isoquinoline-2-carboxylate

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:893566-75-1 SDS

893566-75-1Relevant academic research and scientific papers

AZABENZIMIDAZOLE DERIVATIVES AS PI3K BETA INHIBITORS

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, (2018/01/19)

The present invention relates to azabenzimidazole derivatives of Formula (I) (I) wherein the variables have the meaning defined in the claims. The compounds according to the present invention are useful as pI3Kβ inhibitors. The invention further relates to pharmaceutical compositions comprising said compounds as an active 10 ingredient as well as the use of said compounds as a medicament.

IMIDAZO[1,2-A]PYRIDINE DERIVATIVES AS HISTONE DEMETHYLASE INHIBITORS

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Paragraph 0214-0215, (2018/01/15)

This disclosure relates, inter alia, to compounds that inhibit histone demethylase activity. In particular, the disclosure relates to compounds that inhibit histone lysine demethylase KDM5B, pharmaceutical compositions and methods of use, such as methods of treating cancer using the compounds and pharmaceutical compositions disclosed herein.

SUBSTITUTED NUCLEOSIDE DERIVATIVES USEFUL AS ANTICANCER AGENTS

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Paragraph 0559; 0560, (2016/09/26)

Compounds of the general formula (I): processes for the preparation of these compounds, compositions containing these compounds, and the uses of these compounds.

Certain pyrazoline derivatives with kinase inhibitory activity

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Page/Page column 101; 102, (2008/12/06)

The present invention provides certain pyrazoline compounds useful as inhibitors of protein kinases. The invention also provides pharmaceutical compositions and methods of using the compositions in the treatment of various diseases.

NOVEL COMPOUNDS

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Page/Page column 17; 24-25, (2010/11/08)

The invention provides compounds of formula (I): wherein R1, R2, A, A1 and B are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the ph

NOVEL HYDANTOIN DERIVATIVES AS METALLOPROTEINASE INHIBITORS

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Page/Page column 16; 24, (2010/11/08)

The invention provides compounds of formula (I): wherein R1, R2, A, A1 and B are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the ph

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