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Isoquinolin-6-ylboronic acid hydrochloride (pentahydrate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1236031-63-2

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1236031-63-2 Usage

Uses

Isoquinolin-6-ylboronic acid, HCl

Check Digit Verification of cas no

The CAS Registry Mumber 1236031-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,0,3 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1236031-63:
(9*1)+(8*2)+(7*3)+(6*6)+(5*0)+(4*3)+(3*1)+(2*6)+(1*3)=112
112 % 10 = 2
So 1236031-63-2 is a valid CAS Registry Number.

1236031-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name isoquinolin-6-ylboronic acid hydrochloride

1.2 Other means of identification

Product number -
Other names ISOQUINOLIN-6-YLBORONIC ACID HYDROCHLORIDE (PENTAHYDRATE)

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:1236031-63-2 SDS

1236031-63-2Downstream Products

1236031-63-2Relevant academic research and scientific papers

Rational Design and Integrative Assembly of Heteromeric Metalla[2]Catenanes Featuring Cp*Ir/Rh Fragments

Liu, Dong,Lu, Ye,Lin, Yue-Jian,Jin, Guo-Xin

supporting information, (2022/02/22)

We report a design strategy for integrative assembly of heteromeric [2]catenanes. The design focuses on the shape and functional group match of two different metalla-rectangles. A series of dipyridyl ligands with different lengths, widths and functional groups were designed and used for assembly experiments. Six heteromeric [2]catenanes were obtained both by direct mixture of two pre-assembled metalla-rectangles and one-pot three-component self-assembly. Multiple analytic methods were employed to characterize the catenanes, including single crystal X-ray diffraction analysis, NMR spectroscopy, mass spectroscopy and elemental analysis.

Organic compound and electrochromic element

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Paragraph 0124-0127, (2021/06/22)

The disclosure provides an organic compound and an electrochromic element. The organic compound absorbs light of a wavelength range from 450 nm to 580 nm in a reduction state and is colored, is superior in high-temperature drive durability and is expressed by the following formula [1]. Z1 and Z2 each represent a substituent. R11 to R18 each represent a hydrogen atom or a substituent. R12 and R13 are optionally bound to each other to form a ring. R21 and R22 each represent a hydrogen atom or a substituent. X- represents an anion, and n is an integer greater than or equal to 1. When n is 2 or greater, two or more X-s are the same or different from each other.

FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE

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Page/Page column 171, (2010/08/08)

The invention relates to thiazole compounds of Formula (I) and compositions thereof useful for treating diseases mediated by protein kinase B (PKB) where the variables have the definitions provided herein. The invention also relates to the therapeutic use of such thiazole compounds and compositions thereof in treating disease states associated with abnormal cell growth, cancer, inflammation, and metabolic disorders.

Thiazole compounds and methods of use

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Page/Page column 33, (2008/06/13)

The invention relates to thiazole compounds of Formula I and Formula II and compositions thereof useful for treating diseases mediated by protein kinase B (PKB) where the variables have the definitions provided herein. The invention also relates to the therapeutic use of such thiazole compounds and compositions thereof in treating disease states associated with abnormal cell growth, cancer, inflammation, and metabolic disorders.

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