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458528-08-0

2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 458528-08-0 Structure

  • Basic information

    1. Product Name: 2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester
    2. Synonyms: 2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester
    3. CAS NO:458528-08-0
    4. Molecular Formula:
    5. Molecular Weight: 287.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 458528-08-0.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: 2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester(458528-08-0)
    11. EPA Substance Registry System: 2-trimethylsilanyloxy-azepane-1-carboxylic acid tert-butyl ester(458528-08-0)

  • 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: 458528-08-0(Hazardous Substances Data)

458528-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 458528-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,8,5,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 458528-08:
(8*4)+(7*5)+(6*8)+(5*5)+(4*2)+(3*8)+(2*0)+(1*8)=180
180 % 10 = 0
So 458528-08-0 is a valid CAS Registry Number.

458528-08-0Downstream Products

458528-08-0Relevant articles and documents

The versatile conversion of lactams to the α-alkylated azacycles via cyclic N,O-acetal TMS ether

Suh, Young-Ger,Kim, Seok-Ho,Jung, Jae-Kyung,Shin, Dong-Yun

, p. 3165 - 3167 (2002)

The efficient preparation of the cyclic N,O-acetals from lactams by DIBAL reduction followed by direct trapping of the resulting N,O-hemiacetals using TMSOTf/pyridine system is described. In addition, the facile nucleophilic addition of various carbon nucleophiles at the carbonyl carbons of the lactams through the corresponding N,O-acetals is also reported.

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