Welcome to LookChem.com Sign In|Join Free
  • or
1,2-Benzisoxazole, 3-(2,6-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87828-91-9

Post Buying Request

87828-91-9 Suppliers

Recommended suppliers

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

87828-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87828-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87828-91:
(7*8)+(6*7)+(5*8)+(4*2)+(3*8)+(2*9)+(1*1)=189
189 % 10 = 9
So 87828-91-9 is a valid CAS Registry Number.

87828-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,6-dimethylphenyl)-1,2-benzoxazole

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:87828-91-9 SDS

87828-91-9Downstream Products

87828-91-9Relevant academic research and scientific papers

An improved synthesis of 1,2-benzisoxazoles: TBAF mediated 1,3-dipolar cycloaddition of nitrile oxides and benzyne

Spiteri, Christian,Sharma, Pallavi,Zhang, Fengzhi,MacDonald, Simon J. F.,Keeling, Steve,Moses, John E.

supporting information; experimental part, p. 1272 - 1274 (2010/07/05)

An efficient synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reaction partners medi

An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne

Spiteri, Christian,Mason, Christopher,Zhang, Fengzhi,Ritson, Dougal J.,Sharma, Pallavi,Keeling, Steve,Moses, John E.

experimental part, p. 2537 - 2542 (2010/07/16)

An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reactants simultaneously. The Royal Society of Chemistry 2010.

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 87828-91-9