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4l4-[1,2,4]Oxathiazolo[2,3-b][1,2,4]oxathiazole, 2,6-bis(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62302-11-8

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62302-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62302-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,0 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62302-11:
(7*6)+(6*2)+(5*3)+(4*0)+(3*2)+(2*1)+(1*1)=78
78 % 10 = 8
So 62302-11-8 is a valid CAS Registry Number.

62302-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis-(4-nitro-phenyl)-4λ4-[1,2,4]oxathiazolo[2,3-b][1,2,4]oxathiazole

1.2 Other means of identification

Product number -
Other names 4-nitro-N-[(Z)-5-(4-nitro-phenyl)-[1,2,4]oxathiazol-3-ylidene]-benzamide

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:62302-11-8 SDS

62302-11-8Downstream Products

62302-11-8Relevant academic research and scientific papers

SYNTHESIS OF SYMMETRICAL 1,6-DIHETERO-6aλ4-THIA-3,4-DIAZAPENTALENES FROM 5-AMINO-1,2,3,4-THIATRIAZOLE

Gerrit, L'abbe,Vermeulen, Guido

, p. 89 - 98 (2007/10/02)

1,6-Dioxa-6aλ4-thia-3,4-diazapentalenes 7 and 1,3,4,6-tetraaza-6aλ4-thiapentalenes 15, two new classes of compounds with single bond - no bond resonance, have been prepared by reaction of 5-amino-1,2,3,4-thiatriazole 4 with acyl chlorides and imidoyl chlorides.In the latter case, the salts of 5-imino-Δ3-1,2,4-thiadiazolines 12 were first isolated and subsequently reacted with a second equivalent of imidoyl chloride.This also led to the synthesis of unsimmetrically substituted 1,3,4,6-tetraaza-6aλ4-thiapentalenes.In the presence of bases, the salts 12 decompose via the isolable free bases 13 into N-cyanoamidines 14 and sulfur.Treatment of the dioxathiapentalenes 7 with P4S10, or direct thiobenzoylation of 4 gave the 3,4-diaza-1,6aλ4-trithiapentalenes 9.

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