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CAS

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916152-63-1

(2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 916152-63-1 Structure

  • Basic information

    1. Product Name: (2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine
    2. Synonyms: (2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine
    3. CAS NO:916152-63-1
    4. Molecular Formula:
    5. Molecular Weight: 487.758
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 916152-63-1.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: (2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine(916152-63-1)
    11. EPA Substance Registry System: (2R,5S)-2-(3-Benzyloxy-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-pyrrolidine(916152-63-1)

  • 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: 916152-63-1(Hazardous Substances Data)

916152-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916152-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,1,5 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 916152-63:
(8*9)+(7*1)+(6*6)+(5*1)+(4*5)+(3*2)+(2*6)+(1*3)=161
161 % 10 = 1
So 916152-63-1 is a valid CAS Registry Number.

916152-63-1Relevant articles and documents

Further studies on enantioselective synthesis of (+)-anatoxin-a using enyne metathesis: unexpected inversion of chirality via a skeletal rearrangement of 9-azabicyclo[4.2.1]nonene derivative

Tomita, Tomohiro,Kita, Yoichi,Kitamura, Tsuyoshi,Sato, Yoshihiro,Mori, Miwako

, p. 10518 - 10527 (2006)

The formal total synthesis of (+)-anatoxin-a was accomplished using enyne metathesis as a key step. It is very interesting that (+)-anatoxin-a was synthesized from (S)-pyroglutamic acid via an unusual inversion of chirality, which is rationalized in terms

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