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N-(4-dimethylaminobenzyl)-tert-butylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144261-17-6 Structure
  • Basic information

    1. Product Name: N-(4-dimethylaminobenzyl)-tert-butylamine
    2. Synonyms: N-(4-dimethylaminobenzyl)-tert-butylamine
    3. CAS NO:144261-17-6
    4. Molecular Formula:
    5. Molecular Weight: 206.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144261-17-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(4-dimethylaminobenzyl)-tert-butylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-dimethylaminobenzyl)-tert-butylamine(144261-17-6)
    11. EPA Substance Registry System: N-(4-dimethylaminobenzyl)-tert-butylamine(144261-17-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 144261-17-6(Hazardous Substances Data)

144261-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144261-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144261-17:
(8*1)+(7*4)+(6*4)+(5*2)+(4*6)+(3*1)+(2*1)+(1*7)=106
106 % 10 = 6
So 144261-17-6 is a valid CAS Registry Number.

144261-17-6Relevant articles and documents

H2 cleavage, hydride formation, and catalytic hydrogenation of imines with zinc complexes of C5Me5 and N-heterocyclic carbenes

Jochmann, Phillip,Stephan, Douglas W.

, p. 9831 - 9835 (2013)

Decamethylzincocene, [ZnCp2], reacts with H2 to give the reduced ZnI compound [Zn2Cp2]. In the presence of coordinating and (more efficiently) of non-coordinating N-heterocyclic carbenes (NHCs), the catalytic hydrogenation of imines with H2 is achieved. The monomeric hydride [Zn(Cp)(H)(SIMes)] is presented and its mechanistic implications are considered. Copyright

Zirconium-Catalyzed Imine Hydrogenation via a Frustrated Lewis Pair Mechanism

Flynn, Stephanie R.,Metters, Owen J.,Manners, Ian,Wass, Duncan F.

, p. 847 - 850 (2016)

Zirconium-based frustrated Lewis pairs (FLPs) are active imine hydrogenation catalysts under mild conditions. Complexes of the type [CpR2ZrOMes][B(C6F5)4] utilize the imine substrate itself as the Lewis base component of the FLP. Catalyst performance is a function of ligand structure; in general more bulky, more electron rich cyclopentadienyl derivatives give the best results. However, Cp? derivatives are not catalytically active, being stable after initial heterolytic cleavage of H2; this allows experimental verification of the competence of the zirconocene-imine pair in FLP-type heterolytic H2 cleavage. Enamines and protected nitriles are also hydrogenated if an additional internal phosphine base is used.

Structure-Activity Relationship and Biological Investigation of SR18292 (16), a Suppressor of Glucagon-Induced Glucose Production

Cameron, Michael D.,Griffin, Patrick R.,Kamenecka, Theodore M.,Lin, Hua,Lin, Li,Novick, Scott J.,Puigserver, Pere,Ruiz, Claudia,Sharabi, Kfir,Zhu, Di

supporting information, p. 980 - 990 (2021/02/01)

Despite a myriad of available pharmacotherapies for the treatment of type 2 diabetes (T2D), challenges still exist in achieving glycemic control. Several novel glucose-lowering strategies are currently under clinical investigation, highlighting the need f

Imine hydrogenation by alkylaluminum catalysts

Hatnean, Jillian A.,Thomson, Jordan W.,Chase, Preston A.,Stephan, Douglas W.

supporting information, p. 301 - 303 (2014/01/06)

Di-isobutylaluminum hydride and tri-iso-butylaluminum (DIBAL 1, TIBAL 2) are shown to be efficient hydrogenation catalysts for a variety of imines at 100 °C and 100 atm of H2, operating via a hydroalumination/ hydrogenolysis mechanism.

2,4-SUBSTITUTED PYRIMIDINES AS CYSTEINE PROTEASE INHIBITORS

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Page/Page column 69, (2010/10/20)

Substituted heteroaryl nitrile derivatives of Formula (I) processes for their preparation, pharmaceutical compositions comprising such compounds and use of the compounds as cysteine protease inhibitors are provided.

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