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CAS

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1367878-26-9

(S)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1367878-26-9 Structure

  • Basic information

    1. Product Name: (S)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate
    2. Synonyms: (S)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate
    3. CAS NO:1367878-26-9
    4. Molecular Formula:
    5. Molecular Weight: 507.526
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1367878-26-9.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)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate(1367878-26-9)
    11. EPA Substance Registry System: (S)-tert-butyl 2-(bis(benzyloxy)phosphoryl)-2-diazo-1-phenylethylcarbamate(1367878-26-9)

  • 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: 1367878-26-9(Hazardous Substances Data)

1367878-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1367878-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,7,8,7 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1367878-26:
(9*1)+(8*3)+(7*6)+(6*7)+(5*8)+(4*7)+(3*8)+(2*2)+(1*6)=219
219 % 10 = 9
So 1367878-26-9 is a valid CAS Registry Number.

1367878-26-9Downstream Products

1367878-26-9Relevant articles and documents

Highly efficient asymmetric mannich reaction of dialkyl α-diazomethylphosphonates with N -carbamoyl imines catalyzed by chiral bronsted acids

Zhang, Hui,Wen, Xiaojing,Gan, Lihua,Peng, Yungui

, p. 2126 - 2129 (2012/07/17)

An efficient method involving the first use of chiral phosphoric acids as catalysts in the asymmetric Mannich reaction of dialkyl diazomethylphosphonates and N-carbamoyl imines is developed. With only 0.1 mol % catalyst 1f, the reaction proceeded smoothly and produced the corresponding β-amino-α- diazophosphonate with up to 97% yield and >99% ee.

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