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CAS

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86910-43-2

(1R,1'S)-N-(2'-hydroxy-1'-methylethyl)-1-(p-methoxyphenyl)-2-phenylethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86910-43-2 Structure

  • Basic information

    1. Product Name: (1R,1'S)-N-(2'-hydroxy-1'-methylethyl)-1-(p-methoxyphenyl)-2-phenylethylamine
    2. Synonyms:
    3. CAS NO:86910-43-2
    4. Molecular Formula:
    5. Molecular Weight: 285.386
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86910-43-2.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: (1R,1'S)-N-(2'-hydroxy-1'-methylethyl)-1-(p-methoxyphenyl)-2-phenylethylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,1'S)-N-(2'-hydroxy-1'-methylethyl)-1-(p-methoxyphenyl)-2-phenylethylamine(86910-43-2)
    11. EPA Substance Registry System: (1R,1'S)-N-(2'-hydroxy-1'-methylethyl)-1-(p-methoxyphenyl)-2-phenylethylamine(86910-43-2)

  • 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: 86910-43-2(Hazardous Substances Data)

86910-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86910-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,1 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86910-43:
(7*8)+(6*6)+(5*9)+(4*1)+(3*0)+(2*4)+(1*3)=152
152 % 10 = 2
So 86910-43-2 is a valid CAS Registry Number.

86910-43-2Downstream Products

86910-43-2Relevant articles and documents

Asymmetric α-substituted phenethylamines. II. The enantioselective synthesis of 1-aryl-2-phenylethylamines from L- and D-amino acids by means of 1,3-asymmetric induction

Suzuki,Takahashi

, p. 31 - 40 (2007/10/02)

Optically pure (1S, 1'S)-1-aryl-N-(1'-alkyl-2'-hydroxyethyl)-2-phenylethylamines were synthesized from L-alanine, L-leucine, and L-isoleucine via (S)-2-aminoalkanols and (E)-(S)-N-(1-alkyl-2-hydroxyethyl)arylmethylideneamines. On the other hand, the amine

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