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1227700-45-9

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1227700-45-9 Usage

Uses

Different sources of media describe the Uses of 1227700-45-9 differently. You can refer to the following data:
1. Reagent for coupling reactions 1 MIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings. Suzuki Cross-Coupling with MIDA Boronates
2. Reagent for coupling reactionsMIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings.Suzuki Cross-Coupling with MIDA Boronates

Check Digit Verification of cas no

The CAS Registry Mumber 1227700-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,7,0 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1227700-45:
(9*1)+(8*2)+(7*2)+(6*7)+(5*7)+(4*0)+(3*0)+(2*4)+(1*5)=129
129 % 10 = 9
So 1227700-45-9 is a valid CAS Registry Number.

1227700-45-9 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (723053)  6-Methoxy-2-pyridinylboronicacidMIDAester  

  • 1227700-45-9

  • 723053-1G

  • 534.69CNY

  • Detail
  • Aldrich

  • (723053)  6-Methoxy-2-pyridinylboronicacidMIDAester  

  • 1227700-45-9

  • 723053-5G

  • 2,382.12CNY

  • Detail

1227700-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-methoxypyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione

1.2 Other means of identification

Product number -
Other names 2-(6-Methoxy-2-pyridin-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione

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:1227700-45-9 SDS

1227700-45-9Upstream product

1227700-45-9Relevant articles and documents

Methods for Forming Protected Organoboronic Acids

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Page/Page column 11; 12, (2011/09/14)

Described are methods of forming protected boronic acids that provide in a manner that is straightforward, scalable, and cost-effective a wide variety of building blocks, such as building blocks containing complex and/or pharmaceutically important structures, and/or provide simple or complex protected organoboronic acid building blocks. A first method includes reacting an imino-di-carboxylic acid and an organoboronate salt. A second method includes reacting a N-substituted morpholine dione and an organoboronic acid.

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