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1026938-67-9

[(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-[1-phenyl-meth-(E)-ylidene]-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1026938-67-9 Structure

  • Basic information

    1. Product Name: [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-[1-phenyl-meth-(E)-ylidene]-amine
    2. Synonyms:
    3. CAS NO:1026938-67-9
    4. Molecular Formula:
    5. Molecular Weight: 305.536
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1026938-67-9.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: [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-[1-phenyl-meth-(E)-ylidene]-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-[1-phenyl-meth-(E)-ylidene]-amine(1026938-67-9)
    11. EPA Substance Registry System: [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-[1-phenyl-meth-(E)-ylidene]-amine(1026938-67-9)

  • 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: 1026938-67-9(Hazardous Substances Data)

1026938-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026938-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,9,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1026938-67:
(9*1)+(8*0)+(7*2)+(6*6)+(5*9)+(4*3)+(3*8)+(2*6)+(1*7)=159
159 % 10 = 9
So 1026938-67-9 is a valid CAS Registry Number.

1026938-67-9Relevant articles and documents

Synthesis of (S)- and (R)-1-(2-furyl)alkylamines and (S)- and (R)-α- amino acids through the addition of organometallic reagents to imines derived from (S)-Valinol

Alvaro, Giuseppe,Martelli, Gianluca,Savoia, Diego,Zoffoli, Andrea

, p. 1773 - 1777 (1998)

(S)-1-(2-Furyl)alkylamines were prepared through the addition of organometallic reagents to the imine derived from 2-furaldehyde and (S)- valinol, previous protection of the auxiliary hydroxy group as trimethylsilyl ether, followed by removal of the auxiliary. Then, protection of the primary amine as tosylamide or benzamide and oxidation of the furan ring gave the N- derivatives of (S)-α-amino acids. (R)-N-Benzoylphenylglycine was prepared from the benzaldimine, where the hydroxy group was protected as the tert- butyldimethylsilyl ether, through addition of 2-furyllithium.

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