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14435-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14435-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,3 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14435-92:
(7*1)+(6*4)+(5*4)+(4*3)+(3*5)+(2*9)+(1*2)=98
98 % 10 = 8
So 14435-92-8 is a valid CAS Registry Number.

14435-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name carbonyl azide

1.2 Other means of identification

Product number -
Other names azido ketone

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:14435-92-8 SDS

14435-92-8Relevant articles and documents

The exciting chemistry of tetraazidomethane

Banert, Klaus,Joo, Young-Hyuk,Rueffer, Tobias,Walfort, Bernhard,Lang, Heinrich

, p. 1168 - 1171 (2007)

(Chemical Equation Presented) With a nitrogen content of 93.3%, "perazidomethane(CN12) is highly explosive but nevertheless isolable. The title compound, which is accessible from commercially available trichloroacetonitrile in one step, undergo

Fascinating diazirinone: A violet gas

Zeng, Xiaoqing,Beckers, Helmut,Willner, Helge,Stanton, John F.

, p. 3403 - 3409 (2012)

Diazirinone (cyclic N2CO) recently identified in solid noble gas matrices and in the gas phase by infrared spectroscopy, has now been trapped at -196°C as a neat brownish-yellow solid, and characterized by low-temperature IR and Raman spectroscopy. Evaporation of the solid yields violet gaseous N2CO, which is surprisingly stable in a clean quartz cell. Its decay at room temperature in the dark follows a second-order rate law (k2 = 4.9 × 10-2 L mol-1 s-1) with a half-life of 30 h at an initial pressure of 5 mbar. The visible absorption spectrum of the gas reveals a structured band with the 0-0 transition at 567 nm (17651 cm-1), and its assignment has been made with the aid of theoretical calculations. Cyclic diazirinone that is isolated in solid Ar at 16 K decomposes upon visible light irradiation to yield N2 and CO, but after being exposed to ArF excimer laser irradiation (193 nm) the N=N bond is cleaved and the open-chain isomers NOCN, ONCN, and ONNC are formed. Diazirinone (cyclic N2CO) has been prepared in a neat form as a violet gas. It has a half-life of 30 h at an initial pressure of 5 mbar in a clean quartz container at room temperature, and the substance has been characterized by IR, Raman, and UV/Vis spectroscopy. Copyright

Asymmetric Radical Bicyclization of Allyl Azidoformates via Cobalt(II)-Based Metalloradical Catalysis

Jiang, Huiling,Lang, Kai,Lu, Hongjian,Wojtas, Lukasz,Zhang, X. Peter

supporting information, p. 9164 - 9167 (2017/07/22)

Cobalt(II)-based metalloradical catalysis has been successfully applied to radical bicyclization of allyl azidoformates to construct aziridine/oxazolidinone-fused bicyclic structures. The Co(II) complex of D2-symmetric chiral amidoporphyrin 3,5

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