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57356-48-6

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57356-48-6 Usage

Description

6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime, with the CAS number 57356-48-6, is a yellow solid compound that is primarily utilized in the field of organic synthesis. Its unique chemical structure and properties make it a valuable component in the creation of various organic compounds.

Uses

Used in Organic Synthesis:
6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime is used as a key intermediate in the synthesis of various organic compounds. Its chemical properties allow it to participate in a range of reactions, such as substitution, addition, and condensation, which are essential for the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime is used as a building block for the development of new drugs. Its unique structure can be modified and functionalized to create novel drug candidates with potential therapeutic applications.
Used in Chemical Research:
6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its reactivity and structural features make it an ideal candidate for exploring new chemical transformations and understanding the underlying principles of organic chemistry.
Used in Material Science:
In the field of material science, 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime can be used as a component in the development of new materials with specific properties. Its chemical structure can be tailored to create materials with desired characteristics, such as improved stability, reactivity, or selectivity.
Used in Environmental Applications:
6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime can also be employed in environmental applications, such as the remediation of contaminated sites or the development of eco-friendly processes. Its chemical properties can be harnessed to facilitate the degradation of pollutants or the synthesis of environmentally benign compounds.
Used in Analytical Chemistry:
In analytical chemistry, 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime can be used as a reference compound or a standard for the calibration of analytical instruments. Its well-defined chemical structure and properties make it suitable for validating the performance of various analytical techniques and ensuring accurate measurements.

Check Digit Verification of cas no

The CAS Registry Mumber 57356-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,5 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57356-48:
(7*5)+(6*7)+(5*3)+(4*5)+(3*6)+(2*4)+(1*8)=146
146 % 10 = 6
So 57356-48-6 is a valid CAS Registry Number.

57356-48-6SDS

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 6,7-dinitro-2,3-dihydro-1,4-benzodioxine

1.2 Other means of identification

Product number -
Other names 1,2-dinitro-4,5-ethylenedioxybenzene

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:57356-48-6 SDS

57356-48-6Relevant articles and documents

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.

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