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CAS

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297160-48-6

3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 297160-48-6 Structure

  • Basic information

    1. Product Name: 3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one
    2. Synonyms: 3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one
    3. CAS NO:297160-48-6
    4. Molecular Formula:
    5. Molecular Weight: 332.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 297160-48-6.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: 3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one(297160-48-6)
    11. EPA Substance Registry System: 3,3,8-trimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one(297160-48-6)

  • 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: 297160-48-6(Hazardous Substances Data)

297160-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297160-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,6 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 297160-48:
(8*2)+(7*9)+(6*7)+(5*1)+(4*6)+(3*0)+(2*4)+(1*8)=166
166 % 10 = 6
So 297160-48-6 is a valid CAS Registry Number.

297160-48-6Downstream Products

297160-48-6Relevant articles and documents

An efficient, environmentally benign, and solvent-free protocol for the synthesis of 4-substituted 1,5-benzodiazepines catalyzed by reusable sulfated polyborate

Indalkar, Krishna S.,Patil, Manisha S.,Chaturbhuj, Ganesh U.

, p. 4496 - 4502 (2017)

An efficient and environmentally benign method has been developed for the one-pot solvent-free synthesis of 4-substituted-1,5-benzodiazepines via three-component reaction of o-phenylenediamine, dimedone with a variety of aldehydes catalyzed by sulfated po

Discovery and optimization of a novel Neuromedin B receptor antagonist

Fu, Jiasheng,Shuttleworth, Stephen J.,Connors, Richard V.,Chai, Anne,Coward, Peter

scheme or table, p. 4264 - 4267 (2010/04/29)

The discovery and parallel synthesis of potent, small molecule antagonists of Neuromedin B receptor based on the ary-hexahydro-dibenzodiazepin-1-one core is described.

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