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2733-41-7

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2733-41-7 Usage

General Description

P-NITROBENZAZIDE is a chemical compound used as a high-performance initiator in explosives. It is a primary explosive and a strong oxidizing agent, making it valuable for its ability to rapidly and efficiently initiate explosive reactions. P-NITROBENZAZIDE is highly sensitive to heat, shock, and friction and can explode under certain conditions. Due to its hazardous nature, strict safety protocols and handling procedures are required when working with this chemical. It is primarily used in pyrotechnics and aerospace applications, especially in the ignition of airbags and seatbelt pretensioners.

Check Digit Verification of cas no

The CAS Registry Mumber 2733-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2733-41:
(6*2)+(5*7)+(4*3)+(3*3)+(2*4)+(1*1)=77
77 % 10 = 7
So 2733-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5N4O3/c8-10-9-7(12)5-1-3-6(4-2-5)11(13)14/h1-4,8H/q+1

2733-41-7SDS

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 4-nitrobenzoyl azide

1.2 Other means of identification

Product number -
Other names Benzoyl azide,4-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:2733-41-7 SDS

2733-41-7Relevant articles and documents

Mechanochemical reactions studied by in situ Raman spectroscopy: Base catalysis in liquid-assisted grinding

Tireli, Martina,Juriba?i? Kulcsár, Marina,Cindro, Nikola,Gracin, Davor,Bili?kov, Nikola,Borovina, Mladen,?uri?, Manda,Halasz, Ivan,U?arevi?, Krunoslav

, p. 8058 - 8061 (2015)

In situ Raman spectroscopy was employed to study the course of a mechanochemical nucleophilic substitution on a carbonyl group. We describe evidence of base catalysis, akin to catalysis in solution, achieved by liquid-assisted grinding.

Synthesis of Acyl Phosphoramidates Employing a Modified Staudinger Reaction

Currie, Iain,Sleebs, Brad E.

supporting information, p. 464 - 468 (2021/02/03)

A one-step synthesis of acyl phosphoramidates from a variety of functionalized acyl azides has been developed employing trimethylsilyl chloride as an activating agent in a modified Staudinger reaction. The methodology was further adapted to include the in situ generation of the acyl azides from a diverse selection of carboxylic acids and hydrazide starting synthons. The reaction scope was extended to include the synthesis of imidodiphosphates and the natural product Microcin C.

Direct conversion of carboxylic acids to various nitrogen-containing compounds in the one-pot exploiting curtius rearrangement

Kumar, Arun,Kumar, Naveen,Sharma, Ritika,Bhargava, Gaurav,Mahajan, Dinesh

, p. 11323 - 11334 (2019/09/10)

Herein we report, a single-pot multistep conversion of inactivated carboxylic acids to various N-containing compounds using a common synthetic methodology. The developed methodology rendered the use of carboxylic acids as a direct surrogate of primary amines, for the synthesis of primary ureas, secondary/tertiary ureas, O/S-carbamates, benzoyl ureas, amides, and N-formyls, exploiting the Curtius reaction. This approach has a potential to provide a diversified library of N-containing compounds, starting from a single carboxylic acid, based on the selection of the nucleophile.

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