Welcome to LookChem.com Sign In|Join Free
  • or
5,6-dinitro-2,3-dihydrobenzo[b][1,4]dioxine is a chemical compound characterized by its molecular structure, which features a benzene ring fused with a dioxin ring, and two nitro groups attached at the 5 and 6 positions. 5,6-dinitro-2,3-dihydrobenzo[b][1,4]dioxine is a derivative of benzo[b][1,4]dioxine, with the addition of two nitro groups and a dihydro functional group. It is an organic molecule that can be found in various chemical research and industrial applications, such as in the synthesis of dyes, pharmaceuticals, and other specialty chemicals. Due to its potential reactivity and the presence of nitro groups, it is important to handle 5,6-dinitro-2,3-dihydrobenzo[b][1,4]dioxine with care, following proper safety protocols to minimize risks associated with its use.

59820-94-9

Post Buying Request

59820-94-9 Suppliers

Recommended suppliers

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

59820-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59820-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,2 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59820-94:
(7*5)+(6*9)+(5*8)+(4*2)+(3*0)+(2*9)+(1*4)=159
159 % 10 = 9
So 59820-94-9 is a valid CAS Registry Number.

59820-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dinitro-2,3-dihydrobenzo[b][1,4]dioxine

1.2 Other means of identification

Product number -
Other names 5,6-dinitro-2,3-dihydro-benzo[1,4]dioxin

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:59820-94-9 SDS

59820-94-9Relevant academic research and scientific papers

MULTIPLE D2 A(NTA)GONISTS/H3 ANTAGONISTS FOR TREATMENT OF CNS-RELATED DISORDERS

-

, (2015/05/26)

The present invention relates to compounds compound according to Formula (III); and pharmaceutically acceptable salts, hydrates and solvates thereof. These compounds have D2receptor antagonist/(partial) agonist effects and H3antagonistic effects, pharmaceutical compositions thereof, and methods of using them for application in the prophylaxis or treatment of CNS disorders.

THIAZOLE DERIVATIVES AS PROTEIN KINASE INHIBITORS

-

Page/Page column 79; 80, (2009/06/27)

The present invention relates to novel Thiazole Derivatives, compositions comprising the Thiazole Derivatives, and methods for using the Thiazole Derivatives for treating or preventing a proliferative disorder, an anti-proliferative disorder, inflammation, arthritis, a central nervous system disorder, a cardiovascular disease, alopecia, a neuronal disease, an ischemic injury, a viral infection, a fungal infection, or a disorder related to the activity of a protein kinase.

Influence of the Heterocyclic Side Ring on Orientation During Nitrations of 1,2-Alkylenedioxy-annelated Benzenes and Their Mononitro Derivatives

Takakis, Ioannis M.,Hadjimihalakis, Phaedon M.

, p. 625 - 634 (2007/10/02)

Nitration of 1,2-alkylenedioxybenzenes 1 furnished the respective nitro derivatives 3 and 4 in the relative ratios: 4a:3a/100:trace, 4b:3b/98:2.4, 4c:3c/86:14, 4e:3e/91:9, 4f:3f/99:1.3.Nitration of 4 gave 5a:6a:8a/0:0:100, 5b:6b:8b/7.7:3.2:89, 5c:6c:8c/23:12:65, 5d:6d:8d/14:74:12, 5e:6e:8e/27:18:55 and 5f:6f:8f/23:7.0:70.Nitration of the isomeric 3 afforded the dinitroproducts 5, 6 and 7 in the following relative ratios: 5a:6a:7a/92:8:0, 5b:6b:7b/80:20:0, 5c:6c:7c/69:20:11, 5d:6d:7d/45:19:36, 5e:6e:7e/37:57:5.9 and 5f:6f:7f/64:36:0.Nitration of 3-nitro-1,2-dimethoxybenzene (9) furnished: 10:11/63:37.Orientation as a function of the h eterocyclic ring-size is discussed.

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 59820-94-9