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1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 474328-13-7 Structure
  • Basic information

    1. Product Name: 1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI)
    2. Synonyms: 1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI)
    3. CAS NO:474328-13-7
    4. Molecular Formula: C12H13NO2
    5. Molecular Weight: 203.24
    6. EINECS: N/A
    7. Product Categories: ETHYL
    8. Mol File: 474328-13-7.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: 1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI)(474328-13-7)
    11. EPA Substance Registry System: 1H-2-Benzazepine-1,5(2H)-dione,4-ethyl-3,4-dihydro-(9CI)(474328-13-7)
  • 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: 474328-13-7(Hazardous Substances Data)

474328-13-7 Usage

Chemical Class

Benzazepine

Explanation

The compound belongs to the benzazepine class, which is a group of chemical compounds that have a fused benzene and pyridine ring structure.

Explanation

The molecular weight is the mass of one mole of a substance, expressed in grams per mole (g/mol). For this compound, the molecular weight is 217.26 g/mol.

Explanation

The compound is a heterocyclic organic compound, which means it contains a ring structure with both carbon and other non-carbon atoms (in this case, nitrogen and oxygen).

Explanation

The compound has a seven-membered ring structure, which includes nitrogen and oxygen atoms as part of the ring.

Explanation

The compound contains an ethyl group (C2H5) and a dihydro-1,4-cyclohexadien-1-yl group, which are both functional groups that contribute to its chemical properties.

Explanation

Due to its structural properties and biological activity, the compound has potential applications in the pharmaceutical and medicinal fields. However, further research is needed to determine its specific uses and effects in biological systems.

Explanation

The compound's precise uses and potential effects in biological systems would need to be studied further to fully understand its applications and potential benefits.

Molecular Weight

217.26 g/mol

Heterocyclic Organic Compound

Yes

Ring Structure

Seven-membered ring with nitrogen and oxygen atoms

Functional Groups

Ethyl group and dihydro-1,4-cyclohexadien-1-yl group

Pharmaceutical and Medicinal Applications

Potential

Further Research

Required

Check Digit Verification of cas no

The CAS Registry Mumber 474328-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,3,2 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 474328-13:
(8*4)+(7*7)+(6*4)+(5*3)+(4*2)+(3*8)+(2*1)+(1*3)=157
157 % 10 = 7
So 474328-13-7 is a valid CAS Registry Number.

474328-13-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-3,4-dihydro-2H-2-benzazepine-1,5-dione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:474328-13-7 SDS

474328-13-7Downstream Products

474328-13-7Relevant articles and documents

Photocycloaddition of phthalimide anion to alkenes - A highly efficient, convergent method for [2]benzazepine synthesis

Suau, Rafael,Sanchez-Sanchez, Cristobal,Garcia-Segura, Rafael,Perez-Inestrosa, Ezequiel

, p. 1903 - 1911 (2007/10/03)

The excited state of phthalimide anion adds to cyclic, acyclic and aryl-conjugated alkenes in an efficient and regioselective manner to form [2]benzazepine-1,5-diones, substituted at positions 3 and/or 4. The reaction is independent of the ionization pote

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