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(R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 336850-33-0 Structure
  • Basic information

    1. Product Name: (R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine
    2. Synonyms: (R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine
    3. CAS NO:336850-33-0
    4. Molecular Formula:
    5. Molecular Weight: 372.851
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 336850-33-0.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: (R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine(336850-33-0)
    11. EPA Substance Registry System: (R)-1-(tert-butoxycarbonyl)-2-[α-(benzofuran-2-yl)-(4-chlorophenyl)methyl]hydrazine(336850-33-0)
  • 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: 336850-33-0(Hazardous Substances Data)

336850-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 336850-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,8,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 336850-33:
(8*3)+(7*3)+(6*6)+(5*8)+(4*5)+(3*0)+(2*3)+(1*3)=150
150 % 10 = 0
So 336850-33-0 is a valid CAS Registry Number.

336850-33-0Downstream Products

336850-33-0Relevant articles and documents

Chiral azole derivatives. Part 5: Synthesis of enantiomerically pure 1-[α-(benzofuran-2-yl)arylmethyl]-1H-1,2,4-triazoles, antifungal and antiaromatase agents

Messina, Flavia,Botta, Maurizio,Corelli, Federico,Paladino, Antonella

, p. 4895 - 4901 (2000)

Racemic and enantiopure benzofuranmethanamines 5a-c have been reacted with N-Boc-3-(4-cyanophenyl)oxaziridine to give N-Boc-hydrazines 7a-c, which have in turn been transformed by deprotection and cyclisation into triazoles 4a-c, potent antiaromatase agen

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