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1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169825-32-5 Structure
  • Basic information

    1. Product Name: 1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)
    2. Synonyms: 1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)
    3. CAS NO:169825-32-5
    4. Molecular Formula: C11H11NO3
    5. Molecular Weight: 205.20994
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 169825-32-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 358.7±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.27±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.01±0.40(Predicted)
    10. CAS DataBase Reference: 1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)(169825-32-5)
    12. EPA Substance Registry System: 1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)(169825-32-5)
  • 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: 169825-32-5(Hazardous Substances Data)

169825-32-5 Usage

Derivative of benzazepine

Yes
Benzazepine is a seven-membered ring compound containing one nitrogen atom, and this compound is a derivative of it.

2,5-dihydro-9-methoxy-substituted version

Yes
This indicates that the compound has a methoxy group (-OCH3) attached to the 9th carbon atom and two hydrogen atoms added to the 2nd and 5th positions.

Carbonyl groups

At the 6th and 7th positions
The compound has two carbonyl groups (C=O) present at the 6th and 7th positions in the benzazepine ring.

Pharmacological properties

Potential
The compound may have pharmacological properties, which means it could have an effect on biological systems and may be useful in the development of drugs.

Applications

Medicinal chemistry

Further study and evaluation

Required
The specific properties, uses, and potential effects of this compound would need to be further studied and evaluated to fully understand its potential applications and limitations.

Check Digit Verification of cas no

The CAS Registry Mumber 169825-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,8,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 169825-32:
(8*1)+(7*6)+(6*9)+(5*8)+(4*2)+(3*5)+(2*3)+(1*2)=175
175 % 10 = 5
So 169825-32-5 is a valid CAS Registry Number.

169825-32-5Downstream Products

169825-32-5Relevant articles and documents

Thermal and acid-catalysed sigmatropic rearrangements of allylamino-methoxy-1,2-benzoquinones

Viallon, Loik,Reinaud, Olivia,Capdevielle, Patrice,Maumy, Michel

, p. 13605 - 13614 (2007/10/03)

Thermal and acid-catalysed sigmatropic rearrangements of 4-(N-methyl-N-allylamino)-5-methoxy-1,2-benzoquinones 3 and of 4-(2-vinyl-aziridino or azetidino)-5-methoxy-1,2-benzoquinones 7 were studied and compared. The mechanisms of these reactions are discussed.

Synthesis of Tetrahydroazocino- and Dihydroazepino-1,2-Benzoquinones via Amino-Claisen Rearrangement of 4-(2-Vinyl-Azetidino and Aziridino)-1,2-Benzoquinones

Viallon, Loik,Reinaud, Olivia,Capdevielle, Patrice,Maumy, Michel

, p. 4787 - 4790 (2007/10/02)

Amino-Claisen rearrangement of 4-(2-vinyl-azetidino or aziridino)-5-methoxy-1,2-benzoquinones 3a,b selectively gives rise to the new tetrahydroazocino-quinone 4a or dihydroazepino-quinone 4b respectively.Based on paramethoxyphenol as starting material, overall yields for the 3 steps synthesis of heterobicyclic quinones 4a,b are 58 and 52percent.

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