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145439-39-0

C16H21NO4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145439-39-0 Structure

  • Basic information

    1. Product Name: C16H21NO4S
    2. Synonyms:
    3. CAS NO:145439-39-0
    4. Molecular Formula:
    5. Molecular Weight: 323.413
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145439-39-0.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: C16H21NO4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H21NO4S(145439-39-0)
    11. EPA Substance Registry System: C16H21NO4S(145439-39-0)

  • 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: 145439-39-0(Hazardous Substances Data)

145439-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145439-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,4,3 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145439-39:
(8*1)+(7*4)+(6*5)+(5*4)+(4*3)+(3*9)+(2*3)+(1*9)=140
140 % 10 = 0
So 145439-39-0 is a valid CAS Registry Number.

145439-39-0Downstream Products

145439-39-0Relevant articles and documents

A NOVEL REARRANGEMENT OF TERTIARY α-ALLENIC ALCOHOL CARBAMATES. PREPARATION OF 2-O-CARBAMOYL-4,4-DISUBSTITUTED-1,3-BUTADIENES

Friesen, Richard W.,Kolaczewska, Aleksandra E.,Khazanovich, Nina

, p. 6715 - 6718 (1992)

Treatment of a variety of tertiary α-allenic alcohols with N-tosyl isocyanate results in a facile and novel rearrangement reaction that provides isolable 2-O-carbamoyl-4,4-disubstituted-1,3-butadienes in a stereoselective manner.

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