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13470-20-7

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13470-20-7 Usage

Chemical Properties

dark brown, very hygroscopic crystal(s); prepared by heating uranium turnings in a nitrogen gas stream saturated with bromine vapor; can be purified by vacuum distillation in a similar nitrogen stream [KIR83]

Check Digit Verification of cas no

The CAS Registry Mumber 13470-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13470-20:
(7*1)+(6*3)+(5*4)+(4*7)+(3*0)+(2*2)+(1*0)=77
77 % 10 = 7
So 13470-20-7 is a valid CAS Registry Number.
InChI:InChI=1/4BrH.U/h4*1H;/q;;;;+4/p-4

13470-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Uranium bromide

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:13470-20-7 SDS

13470-20-7Relevant articles and documents

A spatially separated [KBr6]5- anion in the cyanido-bridged uranium(IV) compound [U2(CN)3(NH3)14]5+[KBr6]5-·NH3

Deubner, H. Lars,Kraus, Florian

, p. 111 - 116 (2020)

The reaction of uranium tetrabromide with potassium cyanide in anhydrous liquid ammonia at room temperature leads to the formation of brown crystals of [U2(CN)3(NH3)14]5+ [KBr6]5- · NH3. We determined the crystal structure of the compound by single crystal X-ray diffraction. To the best of our knowledge it contains the unprecedented spatially separated [KBr6]5- anion and presents the first uranium(IV) cyanide compound which forms a layer structure. The compound crystallizes in the trigonal space group P3 m1 (No. 164) with a = 10.3246(13), c = 8.4255(17) ?, V = 777.8(3) ?3, Z = 1 at T = 100 K and is well described with the Niggli formula 2 ∞[U(CN)3/2(NH3)7/1]2[KBr6/1].

Study of the electronic structure of the actinide tetrabromides ThBr4 and UBr4 using ultraviolet photoelectron spectroscopy and density functional calculations

Beeching,Dyke,Morris,Ogden

, p. 9832 - 9839 (2001)

Ultraviolet photoelectron spectroscopy and density functional theory was used to study the electronic structure of actinide tetrabromides. A high temperature photoelectron spectrometer was used to record photoelectron spectra for ThBr4 and UBr4. Vertical ionization energies were calculated for the tetrahalides and supporting matrix isolation experiments were carried out.

Facile Syntheses of pure Uranium(III) Halides: UF3, UCl3, UBr3, and UI3

Rudel, Stefan S.,Deubner, H. Lars,Scheibe, Benjamin,Conrad, Matthias,Kraus, Florian

, p. 323 - 329 (2018/04/05)

Herein we describe a convenient lab scale synthesis for pure and solvent-free binary uranium(III) halides UCl3, UBr3, and UI3. This is achieved by the reduction of the respective uranium(IV) halides with elemental silicon in borosilicate ampoules at moderate temperature. The silicon tetrahalides SiX4 formed as a side product are utilized for the removal of excess starting material via a chemical vapor transport reaction. The syntheses introduced herein avoid the need for pure metallic uranium and are based on uranium(IV) halides synthesized from UO2 and the respective aluminum halides and purified by chemical vapor transport. These uranium(III) halides are obtained in single crystalline form. A similar reaction yields UF3 as a microcrystalline powder. However, no beneficial transport reaction occurs with this halide. Also, a higher temperature has to be applied and steel ampoules have to be used. The identities and purity of the products were checked by powder X-ray diffraction as well as IR spectroscopy. The synthesis of UI3 enabled its crystal structure determination on single crystals for the first time. UI3 crystallizes in the PuBr3 structure type with space group type Cmcm and a = 4.3208(9), b = 13.923(3), c = 9.923(2) ?, V = 596.9(2) ?3, and Z = 4 at T = 100 K.

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