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5-Isoquinolinamine,8-bromo-(9CI) is a chemical compound characterized by the molecular formula C9H8BrN. It is a derivative of isoquinolinamine, a heterocyclic compound with a distinctive bicyclic structure. The unique feature of 5-Isoquinolinamine,8-bromo-(9CI) is the presence of a bromine atom at the 8th position on the isoquinolinamine ring, which may confer specific chemical properties and potential applications.

90721-34-9

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90721-34-9 Usage

Uses

Used in Pharmaceutical Industry:
5-Isoquinolinamine,8-bromo-(9CI) is used as a building block for the synthesis of other compounds in the pharmaceutical industry. Its unique structure, including the bromine atom, may contribute to the development of new drugs with specific therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 90721-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,2 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90721-34:
(7*9)+(6*0)+(5*7)+(4*2)+(3*1)+(2*3)+(1*4)=119
119 % 10 = 9
So 90721-34-9 is a valid CAS Registry Number.

90721-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-bromoisoquinolin-5-amine

1.2 Other means of identification

Product number -
Other names 5-isoquinolinamine,8-bromo

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:90721-34-9 SDS

90721-34-9Relevant academic research and scientific papers

MENIN INHIBITORS AND METHODS OF USE FOR TREATING CANCER

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Paragraph 00600, (2021/10/15)

The present disclosure provides compounds represented by Formula (I): or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, L1, R2 B, Q and E are as defined as set forth in

Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor

-

, (2008/06/13)

Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity, wherein X1, X2, X3, X4, X5, R5, R6, R7, R8a, R8b, R9, Z1, Z2 and L are as defined in the description.

Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor

-

Page/Page column 34, (2010/02/11)

Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity.

Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor

-

, (2008/06/13)

Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity.

Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor

-

, (2008/06/13)

Compounds of formula (I) are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity.

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