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CAS

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133024-37-0

(+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133024-37-0 Structure

  • Basic information

    1. Product Name: (+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene
    2. Synonyms: (+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene
    3. CAS NO:133024-37-0
    4. Molecular Formula:
    5. Molecular Weight: 306.361
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133024-37-0.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: (+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene(133024-37-0)
    11. EPA Substance Registry System: (+/-)-1-benzyloxy-4-(oxiranylmethoxy)naphthalene(133024-37-0)

  • 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: 133024-37-0(Hazardous Substances Data)

133024-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133024-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,2 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133024-37:
(8*1)+(7*3)+(6*3)+(5*0)+(4*2)+(3*4)+(2*3)+(1*7)=80
80 % 10 = 0
So 133024-37-0 is a valid CAS Registry Number.

133024-37-0Downstream Products

133024-37-0Relevant articles and documents

Synthesis of enantiomeric 4-hydroxypropranolols from 1,4-dihydroxynaphthalene

Kumamoto, Takuya,Aoyama, Naho,Nakano, Satoko,Ishikawa, Tsutomu,Narimatsu, Shizuo

, p. 791 - 795 (2007/10/03)

Both (R)- and (S)-enantiomers of 4-hydroxypropranolol were effectively prepared from 1,4-dihydroxynaphthalene in eight steps. The overall yields were around 30%.

Synthesis of potential Naftopidil metabolites

Kutscher,Engel,Fleischhauer,Niebch

, p. 803 - 806 (2007/10/02)

The synthesis of four proposed metabolites 1-4 of Naftopidil, a selective α1-antagonist, is reported. These compounds comprise hydroxylated and demethylated derivatives and a cleavage product of Naftopidil.

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