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1073314-92-7

tert-butyl allyl[2-(hydroxymethyl)allyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1073314-92-7 Structure

  • Basic information

    1. Product Name: tert-butyl allyl[2-(hydroxymethyl)allyl]carbamate
    2. Synonyms:
    3. CAS NO:1073314-92-7
    4. Molecular Formula:
    5. Molecular Weight: 227.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1073314-92-7.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: tert-butyl allyl[2-(hydroxymethyl)allyl]carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl allyl[2-(hydroxymethyl)allyl]carbamate(1073314-92-7)
    11. EPA Substance Registry System: tert-butyl allyl[2-(hydroxymethyl)allyl]carbamate(1073314-92-7)

  • 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: 1073314-92-7(Hazardous Substances Data)

1073314-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073314-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,1 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1073314-92:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*1)+(3*4)+(2*9)+(1*2)=127
127 % 10 = 7
So 1073314-92-7 is a valid CAS Registry Number.

1073314-92-7Downstream Products

1073314-92-7Relevant articles and documents

2-(3-Pyrrolin-1-yl)-1,4-naphthoquinones: Photoactivated alkylating agents

Aponick, Aaron,Dietz, Amber L.,Pearson, William H.

, p. 4264 - 4276 (2008)

The preparation of 2-(3-pyrrolin-1-yl)-1,4-naphthoquinones and a study of their use as photoactivated alkylating agents is reported. The title compounds were easily synthesized by conjugate addition of the corresponding 3-pyrrolines to various naphthoquin

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