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94830-06-5

1H-Isoindole-1,3(2H)-dione, 2-[2-(5-chloro-7-nitro-1H-indol-3-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94830-06-5 Structure

  • Basic information

    1. Product Name: 1H-Isoindole-1,3(2H)-dione, 2-[2-(5-chloro-7-nitro-1H-indol-3-yl)ethyl]-
    2. Synonyms:
    3. CAS NO:94830-06-5
    4. Molecular Formula: C18H12ClN3O4
    5. Molecular Weight: 369.764
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94830-06-5.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: 1H-Isoindole-1,3(2H)-dione, 2-[2-(5-chloro-7-nitro-1H-indol-3-yl)ethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Isoindole-1,3(2H)-dione, 2-[2-(5-chloro-7-nitro-1H-indol-3-yl)ethyl]-(94830-06-5)
    11. EPA Substance Registry System: 1H-Isoindole-1,3(2H)-dione, 2-[2-(5-chloro-7-nitro-1H-indol-3-yl)ethyl]-(94830-06-5)

  • 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: 94830-06-5(Hazardous Substances Data)

94830-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94830-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94830-06:
(7*9)+(6*4)+(5*8)+(4*3)+(3*0)+(2*0)+(1*6)=145
145 % 10 = 5
So 94830-06-5 is a valid CAS Registry Number.

94830-06-5Upstream product

94830-06-5Downstream Products

94830-06-5Relevant articles and documents

INDOLE DERIVATIVES. 126. SUBSTITUTED NITROTRIPTAMINES

Vinograd, L. Kh.,Suvorov, N. N.

, p. 984 - 988 (1984)

A preparative method has been developed for obtaining substituted nitrotryptamines from the corresponding nitrophenylhydrazones of γ-phtalimidobutyraldehyde.

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