Welcome to LookChem.com Sign In|Join Free

CAS

  • or

641144-16-3

Post Buying Request

641144-16-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

641144-16-3 Usage

Uses

Reactant for:Suzuki cross-coupling reactionsPalladium-catalyzed 1,4-addition reactions

Check Digit Verification of cas no

The CAS Registry Mumber 641144-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,1,1,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 641144-16:
(8*6)+(7*4)+(6*1)+(5*1)+(4*4)+(3*4)+(2*1)+(1*6)=123
123 % 10 = 3
So 641144-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H10BBrO2/c16-14-11-7-3-1-5-9(11)13(15(17)18)10-6-2-4-8-12(10)14/h1-8,17-18H

641144-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-Bromoanthracene-9-boronic acid

1.2 Other means of identification

Product number -
Other names (10-bromoanthracen-9-yl)boronic acid

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:641144-16-3 SDS

641144-16-3Relevant articles and documents

Supramolecular structures and spontaneous resolution: The case of ortho-substituted phenylboronic acids

Filthaus, Matthias,Oppel, Iris M.,Bettinger, Holger F.

experimental part, p. 1201 - 1207 (2008/10/09)

The solid state structures of a number of ortho-substituted arylboronic acids, ortho-bromophenyl, ortho-phenylphenyl, pentamethylphenyl, and 10-bromo-9-anthryl, were determined by X-ray diffraction techniques. All boronic acids investigated form dimers in the solid state, but the interconnection of dimers to ribbons differs from that of the parent phenylboronic acid. Pentamethylphenylboronic acid only uses one hydrogen bond but an additional OH-π interaction for connection of dimers, while all others investigated employ two hydrogen bonds for interconnection of dimers to ribbons. 10-Bromo-9-anthrylboronic acid is found to undergo spontaneous resolution of its enantiomers to a racemic conglomerate upon crystallization. The Royal Society of Chemistry.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 641144-16-3