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13599-78-5

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13599-78-5 Usage

Family

Benzothiadiazole

Nitro group position

5th

Usage

Building block in the synthesis of various organic materials

Applications

a. Polymers
b. Dyes
c. Organic electronics
d. Optoelectronics
e. Materials science

Unique structure

Contributes to its versatility in material development

Industrial and technological purposes

Development of new and advanced materials

Check Digit Verification of cas no

The CAS Registry Mumber 13599-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,9 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13599-78:
(7*1)+(6*3)+(5*5)+(4*9)+(3*9)+(2*7)+(1*8)=135
135 % 10 = 5
So 13599-78-5 is a valid CAS Registry Number.

13599-78-5SDS

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 5-nitro-1,2,3-benzothiadiazole

1.2 Other means of identification

Product number -
Other names 1,2,3-Benzothiadiazole,5-nitro

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:13599-78-5 SDS

13599-78-5Downstream Products

13599-78-5Relevant articles and documents

-

Davies,Kirby

, p. 321 (1967)

-

Synthesis method of 1,2,3-diazosulfide compound

-

Paragraph 0077-0080, (2017/11/18)

The invention discloses a synthesis method of a 1,2,3-diazosulfide compound. A o-aminothiophenol compound with a structure shown as a formula (I) and tert-butyl nitrite are taken as raw materials, and are subjected to intramolecular diazo-reaction to obtain the 1,2,3-diazosulfide compound with a structure shown as a formula (II); a reaction equation is as follows (shown in the description), wherein R=hydrogen, fluorine, chlorine, ester group, nitro or methyl. The synthesis method has the beneficial effects that (1) the operation is simple and convenient in a preparation process, an obtained product is easy for after-treatment, and large-scale industrialized production is suitable; (2) reaction conditions are mild; (3) the synthesis cost is lowered; (4) a reaction substrate is high in functional group tolerance, is wide in range and easy to prepare; (5) the reaction is efficient, the yield is high, and the reaction efficiency is higher after reaction amplification; (6) environment pollution is avoided, and environment friendliness is achieved.

7-AMINOFUROPYRIDINE DERIVATIVES

-

Page/Page column 49, (2011/09/15)

Compounds of Formula 1, as shown below and defined herein: pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as tumors driven at least in part by TAK1 or for which an appropriate TAK1 inhibitor is effective. This Abstract is not limiting of the invention.

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