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119345-99-2

1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119345-99-2 Structure

  • Basic information

    1. Product Name: 1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI)
    2. Synonyms: 1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI)
    3. CAS NO:119345-99-2
    4. Molecular Formula: C6H9NO3
    5. Molecular Weight: 143.14056
    6. EINECS: N/A
    7. Product Categories: ALDEHYDE
    8. Mol File: 119345-99-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI)(119345-99-2)
    11. EPA Substance Registry System: 1-Azetidinecarboxaldehyde, 2-(acetyloxy)- (9CI)(119345-99-2)

  • 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: 119345-99-2(Hazardous Substances Data)

119345-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119345-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119345-99:
(8*1)+(7*1)+(6*9)+(5*3)+(4*4)+(3*5)+(2*9)+(1*9)=142
142 % 10 = 2
So 119345-99-2 is a valid CAS Registry Number.

119345-99-2Downstream Products

119345-99-2Relevant articles and documents

A Facile Synthesis of 2-Substituted Azetidines

Shono, Tatsuya,Matsumura, Yoshihiro,Uchida, Kenshi,Nakatani, Fumihiko

, p. 3029 - 3032 (2007/10/02)

A new method for the synthesis of 2-substituted azetidines has been exploited.The method consists of (1) anodic acetoxylation of 1-(p-tolylsulfonyl)azetidine at the 2-position and (2) subsequent nucleophilic substitution of the acetoxyl group with nucleophiles such as trimethylsilyl cyanide, allyltrimethylsilane, 2-acetoxyfuran, and trimethyl phosphite.

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