Welcome to LookChem.com Sign In|Join Free

CAS

  • or

120493-19-8

Post Buying Request

120493-19-8 Suppliers

Recommended suppliersmore

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

120493-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120493-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,9 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120493-19:
(8*1)+(7*2)+(6*0)+(5*4)+(4*9)+(3*3)+(2*1)+(1*9)=98
98 % 10 = 8
So 120493-19-8 is a valid CAS Registry Number.

120493-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-amine

1.2 Other means of identification

Product number -
Other names -

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:120493-19-8 SDS

120493-19-8Relevant articles and documents

RING FORMATION REACTIONS OF 4-AMINOFURAZAN-3-CARBOXYAMIDOXIMES

Andrianov, V. G.,Rozhkov, E. N.,Eremeev, A. V.

, p. 470 - 474 (1994)

The ring formation of 4-aminofurazan-3-carboxamidoximes in the reaction with the orthoesters and derivatives of formic and acetic acids leads to the closure of the 1,2,4-hydroxydiazole as well as the pyrimidine ring.

Furazans with Azo Linkages: Stable CHNO Energetic Materials with High Densities, Highly Energetic Performance, and Low Impact and Friction Sensitivities

Qu, Yanyang,Zeng, Qun,Wang, Jun,Ma, Qing,Li, Hongzhen,Li, Haibo,Yang, Guangcheng

, p. 12527 - 12532 (2016)

Various highly energetic azofurazan derivatives were synthesized by simple and efficient chemical routes. These nitrogen-rich materials were fully characterized by FTIR spectroscopy, elemental analysis, multinuclear NMR spectroscopy, and high-resolution mass spectrometry. Four of them were further confirmed structurally by single-crystal X-ray diffraction. These compounds exhibit high densities, ranging from 1.62 g cm?3up to a remarkably high 2.12 g cm?3for nitramine-substituted azofurazan DDAzF (2), which is the highest yet reported for an azofurazan-based CHNO energetic compound and is a consequence of the formation of strong intermolecular hydrogen-bonding networks. From the heats of formation, calculated with Gaussian 09, and the experimentally determined densities, the energetic performances (detonation pressure and velocities) of the materials were ascertained with EXPLO5 v6.02. The results suggest that azofurazan derivatives exhibit excellent detonation properties (detonation pressures of 21.8–46.1 GPa and detonation velocities of 6602–10 114 m s?1) and relatively low impact and friction sensitivities (6.0–80 J and 80–360 N, respectively). In particular, they have low electrostatic spark sensitivities (0.13–1.05 J). These properties, together with their high nitrogen contents, make them potential candidates as mechanically insensitive energetic materials with high-explosive performance.

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

What can I do for you?
Get Best Price

Get Best Price for 120493-19-8