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CAS

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70178-04-0

4-(4-nitro-benzoylamino)-isoindole-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 70178-04-0 Structure

  • Basic information

    1. Product Name: 4-(4-nitro-benzoylamino)-isoindole-1,3-dione
    2. Synonyms:
    3. CAS NO:70178-04-0
    4. Molecular Formula:
    5. Molecular Weight: 311.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70178-04-0.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: 4-(4-nitro-benzoylamino)-isoindole-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-nitro-benzoylamino)-isoindole-1,3-dione(70178-04-0)
    11. EPA Substance Registry System: 4-(4-nitro-benzoylamino)-isoindole-1,3-dione(70178-04-0)

  • 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: 70178-04-0(Hazardous Substances Data)

70178-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70178-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70178-04:
(7*7)+(6*0)+(5*1)+(4*7)+(3*8)+(2*0)+(1*4)=110
110 % 10 = 0
So 70178-04-0 is a valid CAS Registry Number.

70178-04-0Downstream Products

70178-04-0Relevant articles and documents

Synthesis of 2-substituted 4-quinazolone-5-carboxylic acids as inhibitors of DNA-gyrase

Sui, Zhihua,Nguyen, Van N.,Fernandez, Jeff,Barrett, John F.,Ohemeng, Kwasi A.

, p. 153 - 156 (1997)

A series of 4-quinazolone-5-carboxylic acids were designed as bacterial DNA gyrase inhibitors. The syntheses of the target compounds were accomplished by reacting 3-aminophthalimide with aroyl chlorides followed by rearrangement of the resulting 3-acylami

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