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CAS

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131704-05-7

trans-N,N-dimethyl-2,3-dihydro-1-(4-methoxyphenoxy)indene-2-methanamine oxalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131704-05-7 Structure

  • Basic information

    1. Product Name: trans-N,N-dimethyl-2,3-dihydro-1-(4-methoxyphenoxy)indene-2-methanamine oxalate
    2. Synonyms:
    3. CAS NO:131704-05-7
    4. Molecular Formula:
    5. Molecular Weight: 387.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131704-05-7.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: trans-N,N-dimethyl-2,3-dihydro-1-(4-methoxyphenoxy)indene-2-methanamine oxalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-N,N-dimethyl-2,3-dihydro-1-(4-methoxyphenoxy)indene-2-methanamine oxalate(131704-05-7)
    11. EPA Substance Registry System: trans-N,N-dimethyl-2,3-dihydro-1-(4-methoxyphenoxy)indene-2-methanamine oxalate(131704-05-7)

  • 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: 131704-05-7(Hazardous Substances Data)

131704-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131704-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,0 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131704-05:
(8*1)+(7*3)+(6*1)+(5*7)+(4*0)+(3*4)+(2*0)+(1*5)=87
87 % 10 = 7
So 131704-05-7 is a valid CAS Registry Number.

131704-05-7Downstream Products

131704-05-7Relevant articles and documents

The Mitsunobu Reaction of Some Indan Amino Alcolhols

Freedman, Jules,Vaal, Mark J.,Huber, Edward W.

, p. 670 - 672 (1991)

The Mitsunobu reaction, utilizing several phenols, has been applied to a series of indan amino alcohols.An interesting example of configurational retention as a result of an aziridinium intermediate was discovered.

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