Welcome to LookChem.com Sign In|Join Free

CAS

  • or

59689-21-3

Post Buying Request

59689-21-3 Suppliers

Recommended suppliersmore

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

59689-21-3 Usage

Chemical compound

2H-3,1-Benzoxazine, 1,4-dihydro-

Class

Benzoxazines

Structure

1,4-dihydrobenzoxazine

Composition

Contains a benzene ring fused to an oxazine ring

Application

Studied for use as monomers for polymer synthesis and building blocks for bioactive molecules

Derivatives

Investigated for potential anti-tumor and anti-inflammatory properties

Check Digit Verification of cas no

The CAS Registry Mumber 59689-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,8 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59689-21:
(7*5)+(6*9)+(5*6)+(4*8)+(3*9)+(2*2)+(1*1)=183
183 % 10 = 3
So 59689-21-3 is a valid CAS Registry Number.

59689-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dihydro-1H-3,1-benzoxazine

1.2 Other means of identification

Product number -
Other names 1,4-dihydro-2H-benz[d][1,3]oxazine

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:59689-21-3 SDS

59689-21-3Downstream Products

59689-21-3Relevant articles and documents

A modified procedure for the deprotection of methoxymethyl ether

Yu, Chengzhi,Liu, Bin,Hu, Longqin

, p. 819 - 822 (2000)

A new modified procedure using a combination of catechol boron bromide with acetic acid was developed to deprotect methoxymethyl group to form 1,3- diols and 1,3-aminoalcohols. (C) 2000 Elsevier Science Ltd.

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 59689-21-3