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93272-83-4

3H-Indol-5-amine, 2,3,3-trimethyl-N-[(4-nitrophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93272-83-4 Structure

  • Basic information

    1. Product Name: 3H-Indol-5-amine, 2,3,3-trimethyl-N-[(4-nitrophenyl)methylene]-
    2. Synonyms:
    3. CAS NO:93272-83-4
    4. Molecular Formula: C18H17N3O2
    5. Molecular Weight: 307.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93272-83-4.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: 3H-Indol-5-amine, 2,3,3-trimethyl-N-[(4-nitrophenyl)methylene]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3H-Indol-5-amine, 2,3,3-trimethyl-N-[(4-nitrophenyl)methylene]-(93272-83-4)
    11. EPA Substance Registry System: 3H-Indol-5-amine, 2,3,3-trimethyl-N-[(4-nitrophenyl)methylene]-(93272-83-4)

  • 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: 93272-83-4(Hazardous Substances Data)

93272-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93272-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,7 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93272-83:
(7*9)+(6*3)+(5*2)+(4*7)+(3*2)+(2*8)+(1*3)=144
144 % 10 = 4
So 93272-83-4 is a valid CAS Registry Number.

93272-83-4Relevant articles and documents

INTERACTION OF 5-AMINO-2,3,3-TRIMETHYL-3H-INDOLE WITH p-NITROBENZALDEHYDE

Lyubich, M. S.,Isaev, Sh. G.,Al'perovich, M. A.,Shpileva, I. S.,Arshava, B. M.

, p. 976 - 977 (1984)

The reaction of 5-amino-2,3,3-trimethyl-3H-indole with p-nitrobenzaldehyde may take place in two directions, depending on the temperature: with the formation of a Schiff's base or of the corresponding styryl compound.

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