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5-Fluoro-2-nitrobenzeneboronic acid pinacol ester, 96% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

925207-14-3

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925207-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 925207-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,2,0 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 925207-14:
(8*9)+(7*2)+(6*5)+(5*2)+(4*0)+(3*7)+(2*1)+(1*4)=153
153 % 10 = 3
So 925207-14-3 is a valid CAS Registry Number.

925207-14-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H62813)  5-Fluoro-2-nitrobenzeneboronic acid pinacol ester, 96%   

  • 925207-14-3

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H62813)  5-Fluoro-2-nitrobenzeneboronic acid pinacol ester, 96%   

  • 925207-14-3

  • 1g

  • 4402.0CNY

  • Detail

925207-14-3SDS

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-(5-Fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan e

1.2 Other means of identification

Product number -
Other names -

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:925207-14-3 SDS

925207-14-3Downstream Products

925207-14-3Relevant articles and documents

Compounds and methods for inhibiting phosphate transport

-

, (2016/05/02)

Compounds having activity as phosphate transport inhibitors, more specifically, inhibitors of intestinal apical membrane Na/phosphate co-transport, are disclosed. The compounds have the following structure (I): including stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, wherein X, Y, A, R1 and R2 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.

Promoting reductive tandem reactions of nitrostyrenes with Mo(CO)6 and a palladium catalyst to produce 3 h -indoles

Jana, Navendu,Zhou, Fei,Driver, Tom G.

supporting information, p. 6738 - 6741 (2015/06/16)

The combination of Mo(CO)6 and 10 mol % of palladium acetate catalyzes the transformation of 2-nitroarenes to 3H-indoles through a tandem cyclization-[1,2] shift reaction of in situ generated nitrosoarenes. Mo(CO)6 appears to have dual roles in this transformation: generate CO and promote C-N bond formation to increase the yield of the N-heterocycle product.

Synthetic strategies to a telomere-targeted pentacyclic heteroaromatic salt

Hutchinson, Ian,Stevens, Malcolm F. G.

, p. 114 - 120 (2008/03/14)

Three routes have been explored to synthesise the telomere-targeted agent 3,11-difluoro-6,8,13-trimethyl-8H-quino[4,3,2-kl]acridinium methosulfate 3. Application of a 6-(2-azidophenyl)phenanthridine precursor 11 gave an entry to the indazolo[2,3-f]phenant

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