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511292-99-2

(TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 511292-99-2 Structure

  • Basic information

    1. Product Name: (TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM
    2. Synonyms: TRIS(ETHYLMETHYLAMIDO)(TERT-BUTYLIMIDO)TANTALUM(V);TRIS(ETHYLMETHYLAMINO)-TERT-BUTYLAMIDO TANTALUM;(TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM
    3. CAS NO:511292-99-2
    4. Molecular Formula: C13H33N4Ta
    5. Molecular Weight: 426.38
    6. EINECS: N/A
    7. Product Categories: TantalumVapor Deposition Precursors;Catalysis and Inorganic Chemistry;Chemical Synthesis;Precursors by Metal;Tantalum
    8. Mol File: 511292-99-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: 64 °F
    4. Appearance: yellow/liquid
    5. Density: 1.323 g/mL at 21 °C(lit.)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Sensitive: air sensitive, moisture sensitiv
    10. CAS DataBase Reference: (TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM(CAS DataBase Reference)
    11. NIST Chemistry Reference: (TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM(511292-99-2)
    12. EPA Substance Registry System: (TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM(511292-99-2)

  • Safety Data

    1. Hazard Codes: C
    2. Statements: 10-14/15-34
    3. Safety Statements: 26-36/37/39-43-45
    4. RIDADR: UN 3398 4.3/PG 2
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 511292-99-2(Hazardous Substances Data)

511292-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 511292-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,2,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 511292-99:
(8*5)+(7*1)+(6*1)+(5*2)+(4*9)+(3*2)+(2*9)+(1*9)=132
132 % 10 = 2
So 511292-99-2 is a valid CAS Registry Number.

511292-99-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail

  • Aldrich

  • (J100043)  Tris(ethylmethylamido)(tert-butylimido)tantalum(V)  electronic grade, ≥95% (CP), ≥99.99% trace metals basis

  • 511292-99-2

  • J100043-5G

  • 2,204.28CNY

  • Detail

511292-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (TERT-BUTYLIMIDO)TRIS(ETHYLMETHYLAMINO)TANTALUM

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:511292-99-2 SDS

511292-99-2Relevant articles and documents

PROCESSES FOR PRODUCING TRANSITION METAL AMIDES

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Page/Page column 2, (2011/02/18)

Processes are provided for producing transition metal amides. In methods according to this invention, at least a halogenated transition metal and an amine are combined in a solvent to produce an intermediate composition and an alkylated metal or a Grignard reagent is added to the intermediate composition to produce the transition metal amide.

Preparation of metal imino/amino complexes for metal oxide and metal nitride thin films

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, (2008/06/13)

This invention relates to an improved process to produce metal imino/amino complexes having the formula R1N=M(NR2R3)3where M is a pentavalent metal or (R1N=)2M′(NR2R3)2where M′ is a hexavalent metal. In the process MX5and two-equivalents of primary amine R1NH2or metal hexahalide, M′X6with seven-equivalents of primary amine H2NR1are reacted in the presence of excess pyridine. The resulting reaction product R1N═MX3(py)2or [(R1N)2M′X2(py)]2then is followed by the addition of LiNR2R3. The process provides the final product in high yield and in high purity as well as representing a simplified procedure for synthesizing R1N═M(NR2R3)3or (R1N═)2M′(NR2R3)2type complexes.

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