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(R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile is a complex chemical compound characterized by its chiral nature, featuring an (R)-enantiomer. It consists of a benzyl group, a tetrahydrobenzodiazepine ring, and a carbonitrile functional group. Due to its structural resemblance to benzodiazepines, this compound may exhibit pharmacological properties such as sedation, anxiety reduction, and muscle relaxation. The carbonitrile group also indicates potential reactivity and utility in the synthesis of other compounds.

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  • 195984-91-9 Structure
  • Basic information

    1. Product Name: (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile
    2. Synonyms: (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile
    3. CAS NO:195984-91-9
    4. Molecular Formula: C21H21N5
    5. Molecular Weight: 343
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 195984-91-9.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: (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile(195984-91-9)
    11. EPA Substance Registry System: (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile(195984-91-9)
  • 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: 195984-91-9(Hazardous Substances Data)

195984-91-9 Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile is used as a potential therapeutic agent for various conditions due to its structural similarity to benzodiazepines. Its application is based on the expectation that it may provide sedative, anxiolytic, and muscle relaxant effects.
Used in Chemical Synthesis:
In the chemical industry, (R)-1-((1H-iMidazol-5-yl)Methyl)-3-benzyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile is used as a precursor compound for the synthesis of other complex molecules. The presence of the carbonitrile group allows for further chemical reactions, making it a versatile building block in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 195984-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,9,8 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 195984-91:
(8*1)+(7*9)+(6*5)+(5*9)+(4*8)+(3*4)+(2*9)+(1*1)=209
209 % 10 = 9
So 195984-91-9 is a valid CAS Registry Number.

195984-91-9Relevant articles and documents

Discovery of (R)-7-cyano-2,3,4,5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-3-(phenylmethyl)-4- (2-thienysulfonyl)-1H-1,4-benzodiazepine (BMS-214662), a farnesyltransferase inhibitor with potent preclinical antitumor activity

Hunt,Ding,Batorsky,Bednarz,Bhide,Cho,Chong,Chao,Gullo-Brown,Guo,Soong Hoon Kim,Lee,Leftheris,Miller,Mitt,Patel,Penhallow,Ricca,Rose,Schmidt,Slusarchyk,Vite,Manne

, p. 3587 - 3595 (2007/10/03)

Continuing structure-activity studies were performed on the 2,3,4,5-tetrahydro-1-(imidazol-4-ylalkyl)-1,4-benzodiazepine farnesyltransferase (FT) inhibitors. These studies demonstrated that a 3(R)-phenylmethyl group, a hydrophilic 7-cyano group, and a 4-s

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