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1243312-43-7

1243312-43-7

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1243312-43-7 Usage

Uses

3-Methoxy-4-pyridineboronic Acid Pinacol Ester is used in preparation of pyrazoles and triazoles as inhibitors of SARM1.

Check Digit Verification of cas no

The CAS Registry Mumber 1243312-43-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,3,1 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1243312-43:
(9*1)+(8*2)+(7*4)+(6*3)+(5*3)+(4*1)+(3*2)+(2*4)+(1*3)=107
107 % 10 = 7
So 1243312-43-7 is a valid CAS Registry Number.

1243312-43-7 Well-known Company Product Price

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  • Aldrich

  • (717665)  3-Methoxy-4-pyridineboronicacidpinacolester  97%

  • 1243312-43-7

  • 717665-1G

  • 1,529.19CNY

  • Detail

  • Aldrich

  • (717665)  3-Methoxy-4-pyridineboronicacidpinacolester  97%

  • 1243312-43-7

  • 717665-5G

  • 5,281.38CNY

  • Detail

1243312-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,3-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)

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:1243312-43-7 SDS

1243312-43-7Relevant articles and documents

Preparation method of 2,3'-dimethoxy-[2,4']bipyridine

-

Paragraph 0027, (2019/08/20)

The invention discloses a preparation method of 2,3'-dimethoxy-[2,4']bipyridine. The preparation method comprises the following steps: performing a reaction on 3-methoxypyridine and a reagent A underthe alkaline conditions at -100 to 80 DEG C so as to obtain 3-methoxy-4-R-pyridine, and performing a reaction on 3-methoxy-4-R-pyridine and 2-bromo-3-methoxypyridine under the alkaline conditions under the catalysis action of a catalyst at -20 to 180 DEG C so as to prepare 2,3'-dimethoxy-[2,4']bipyridine. The preparation method of 2,3'-dimethoxy-[2,4']bipyridine has the advantages of a high yieldand cheap and easily available raw materials, and is suitable for large-scale production.

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