Welcome to LookChem.com Sign In|Join Free
  • or
Carbamic acid, [4-(2-benzofuranyl)phenyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

239088-84-7

Post Buying Request

239088-84-7 Suppliers

Recommended suppliers

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

239088-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 239088-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,9,0,8 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 239088-84:
(8*2)+(7*3)+(6*9)+(5*0)+(4*8)+(3*8)+(2*8)+(1*4)=167
167 % 10 = 7
So 239088-84-7 is a valid CAS Registry Number.

239088-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<(4'-Boc-amino)phenyl>benzo<b>furan

1.2 Other means of identification

Product number -
Other names (4-Benzofuran-2-yl-phenyl)-carbamic acid tert-butyl ester

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:239088-84-7 SDS

239088-84-7Downstream Products

239088-84-7Relevant academic research and scientific papers

BIARYL COMPOUNDS HAVING ANTI-INFECTIVE ACTIVITY

-

Page/Page column 23; 24, (2008/06/13)

Aromatic compounds exemplified by exhibit antimicrobial activity.

An efficient procedure for the synthesis of crystalline aryldiazonium trifluoroacetates - Synthetic applications

Colas, Christophe,Goeldner, Maurice

, p. 1357 - 1366 (2007/10/03)

We have developed a very mild procedure for the synthesis of crystalline aryldiazonium trifluoroacetate salts in high yields under anhydrous conditions. Over thirty mono- or polyfunctional aniline derivatives have been diazotized by this method, including water- and acid-sensitive substrates. The o- and p-hydroxyaryldiazonium salts, derived from the corresponding anilines, could be deprotonated by treatment with K2CO3 to yield pure diazoquinones. NMR and UV/Vis spectra have been recorded for all the synthesized salts; the data are in good agreement with the rather limited published data and constitute a first extensive report of 13C-NMR chemical shifts in diazonium salts. An excellent linear relationship emerged between Brown's substituent constants S+(p) and the 13C(ipso) chemical shifts. The diazonium salts obtained proved to be much more soluble in organic solvents than their tetrafluoroborate counterparts. They were tested in Pd-mediated coupling reactions of various carbon-carbon double bonds, and were found to give good yields within short reaction times under very mild conditions. We believe that diazonium trifluoroacetates represent a very attractive alternative to diazonium tetrafluoroborates.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 239088-84-7