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CAS

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1030592-47-2

2-(2,5-dimethoxyphenyl)-4-(2-hydroxyphenyl)-2,3-dihydro-1H-1,5-benzodiazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1030592-47-2 Structure

  • Basic information

    1. Product Name: 2-(2,5-dimethoxyphenyl)-4-(2-hydroxyphenyl)-2,3-dihydro-1H-1,5-benzodiazepine
    2. Synonyms:
    3. CAS NO:1030592-47-2
    4. Molecular Formula:
    5. Molecular Weight: 374.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1030592-47-2.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: 2-(2,5-dimethoxyphenyl)-4-(2-hydroxyphenyl)-2,3-dihydro-1H-1,5-benzodiazepine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,5-dimethoxyphenyl)-4-(2-hydroxyphenyl)-2,3-dihydro-1H-1,5-benzodiazepine(1030592-47-2)
    11. EPA Substance Registry System: 2-(2,5-dimethoxyphenyl)-4-(2-hydroxyphenyl)-2,3-dihydro-1H-1,5-benzodiazepine(1030592-47-2)

  • 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: 1030592-47-2(Hazardous Substances Data)

1030592-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1030592-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,5,9 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1030592-47:
(9*1)+(8*0)+(7*3)+(6*0)+(5*5)+(4*9)+(3*2)+(2*4)+(1*7)=112
112 % 10 = 2
So 1030592-47-2 is a valid CAS Registry Number.

1030592-47-2Downstream Products

1030592-47-2Relevant articles and documents

Synthesis of 1,5-benzodiazepines with unusual substitution pattern from chalcones under solvent-free microwave irradiation conditions

Escobar, Carlos A.,Donoso-Tauda, Oscar,Araya-Maturana, Ramiro,Sicker, Dieter

experimental part, p. 166 - 174 (2009/04/07)

1,5-Benzodiazepines have been synthesized from the corresponding 2'-hydroxychalcones [1-(2-hydroxyphenyl)-3-aryl-2-propen-1-ones] and o-phenylenediamine, both in methanol, under reflux and under solvent-free microwave irradiation conditions on alumina. Th

4-(2-Hydroxy-phen-yl)-2-phenyl-2,3-dihydro-1H-1,5-benzodiazepine and the 2-(2,3-dimethoxy-phen-yl)-, 2-(3,4-dimethoxy-phen-yl)- and 2-(2,5-dimeth-oxy- phen-yl)-substituted derivatives

Escobar, Carlos A.,Donoso-Tauda, Oscar,Araya-Maturana, Ramiro,Vega, Andres

, p. o426-o430 (2008/09/18)

The 1,5-benzodiazepine ring system exhibits a puckered boat-like conformation for all four title compounds [4-(2-hydroxy-phen-yl)-2-phenyl-2,3- dihydro-1H-1,5-benzodiazepine, C21H18N2O, (I), 2-(2,3-dimethoxy-phen-yl)-4-(2- hydroxy-phen-yl)-2,3-dihydro-1H-

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