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N-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 956434-21-2 Structure
  • Basic information

    1. Product Name: N-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine
    2. Synonyms: N-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine
    3. CAS NO:956434-21-2
    4. Molecular Formula:
    5. Molecular Weight: 279.498
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 956434-21-2.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-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine(956434-21-2)
    11. EPA Substance Registry System: N-benzyl-2-{[tert-butyl(dimethyl)silyl]oxy}propan-1-amine(956434-21-2)
  • 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: 956434-21-2(Hazardous Substances Data)

956434-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956434-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,4,3 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 956434-21:
(8*9)+(7*5)+(6*6)+(5*4)+(4*3)+(3*4)+(2*2)+(1*1)=192
192 % 10 = 2
So 956434-21-2 is a valid CAS Registry Number.

956434-21-2Relevant articles and documents

Syntheses of five- and seven-membered ring sultam derivatives by Michael addition and Baylis-Hillman reactions

Tong, Kun,Tu, Jinchang,Qi, Xueyong,Wang, Min,Wang, Yanjie,Fu, Haizhen,Pittman Jr., Charles U.,Zhou, Aihua

, p. 2369 - 2375 (2013)

Five- and seven-membered sultam derivatives were conveniently synthesized via intra- or intermolecular Michael additions and an improved vinyl sulfonamide Baylis-Hillman reaction. Two different cyclization pathways were explored for the oxa-Michael reaction. A good solvent was discovered for an otherwise sluggish ketone-type Baylis-Hillman reaction in which vinyl sulfonamide ketones were used as the precursors. Furthermore, a strong base caused vinyl sulfonamide ketones to undergo 5-endo-trig intramolecular cyclizations, which are disfavored according to Baldwin's rule. Finally Baylis-Hillman reaction products were used as scaffolds for diversity-oriented sultam syntheses.

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