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850568-65-9

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850568-65-9 Usage

General Description

1-Boc-6-methoxyindole-2-boronic acid is a chemical compound that consists of a boronic acid group connected to a 6-methoxyindole ring, with a tert-butoxycarbonyl (Boc) protecting group attached to the nitrogen atom of the indole ring. 1-Boc-6-methoxyindole-2-boronic acid is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various biologically active molecules. It is also utilized in the development of pharmaceuticals and agrochemicals. The boronic acid functionality in 1-Boc-6-methoxyindole-2-boronic acid makes it a valuable reagent for Suzuki-Miyaura cross-coupling reactions and other types of organic transformations, allowing for the construction of complex molecular structures.

Check Digit Verification of cas no

The CAS Registry Mumber 850568-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 850568-65:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*8)+(2*6)+(1*5)=189
189 % 10 = 9
So 850568-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18BNO5/c1-14(2,3)21-13(17)16-11-8-10(20-4)6-5-9(11)7-12(16)15(18)19/h5-8,18-19H,1-4H3

850568-65-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52482)  1-Boc-6-methoxyindole-2-boronic acid, 98%   

  • 850568-65-9

  • 250mg

  • 926.0CNY

  • Detail
  • Alfa Aesar

  • (H52482)  1-Boc-6-methoxyindole-2-boronic acid, 98%   

  • 850568-65-9

  • 1g

  • 2964.0CNY

  • Detail

850568-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-(tert-Butoxycarbonyl)-6-methoxy-1H-indol-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names [6-methoxy-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-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:850568-65-9 SDS

850568-65-9Relevant articles and documents

Trisoxazoline/Cu(II)-catalyzed asymmetric intramolecular Friedel-Crafts alkylation reaction of indoles

Zhou, Jiao-Long,Ye, Meng-Chun,Sun, Xiu-Li,Tang, Yong

supporting information; experimental part, p. 6877 - 6881 (2009/12/06)

Intramolecular Friedel-Crafts alkylation reaction of indoles catalyzed by trisoxazoline/copper(II) is described. This annulation provides an easy access to polycyclic indole derivatives with up to 90% ee in up to 99% yield.

METHODS FOR TREATING HEPATITIS C

-

Page/Page column 450, (2010/10/20)

In accordance with the present invention, compounds that inhibit viral replication, preferably Hepatitis C Virus (HCV) replication, have been identified, and methods for their use provided. In one aspect of the invention, compounds useful in the treatment

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